--- title: "MAX A67D (c.200C>A, rs786202340) | Dante Labs" description: "ClinVar classifies MAX A67D as Pathogenic/likely pathogenic (criteria provided, multiple submitters, no conflicts). Where it sits in the genome, its predicted effect, and the Genome Test reports that look at it." url: "https://dantelabs.com/genes/max/variants/a67d" --- 1. [Genes](https://dantelabs.com/genes) 2. [MAX](https://dantelabs.com/genes/max) 3. MAX A67D Variant # MAX A67D NM_002382.5(MAX):c.200C>A (p.Ala67Asp) Also known as - p.Ala67Asp - p.A67D - rs786202340 * ClinVar classification Pathogenic/likely pathogenic * Review status 2 stars out of 4 criteria provided, multiple submitters, no conflicts * Last evaluated 27 January 2026 Data current to ClinVar release 2026-10-12 · Dante Labs data release 2026.10.16-c6eea6bf Facts last changed 16 October 2026 ## Summary A67D is a missense variant in MAX: it changes a single amino acid in the protein the gene encodes. ClinVar classifies it as pathogenic or likely pathogenic for Hereditary pheochromocytoma-paraganglioma (criteria provided, multiple submitters, no conflicts). ## ClinVar classifications | Condition | Classification | Review status | Submissions | Last evaluated | | --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- | ---------------------------- | --------------------------------------------------------------------- | ------------- | --------------- | | [Hereditary pheochromocytoma-paraganglioma](https://dantelabs.com/conditions/hereditary-pheochromocytoma-paraganglioma) [ClinVar VCV000185646 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/clinvar/variation/185646/) | Pathogenic/likely pathogenic | 2 stars out of 4 criteria provided, multiple submitters, no conflicts | 2 submissions | 27 January 2026 | Classifications as ClinVar records them in release 2026-10-12. ClinVar updates them as evidence is reviewed. ## Where it lies in MAX A67D lies in exon 4 of the 5 in MAX's MANE Select transcript, NM_002382.5. [MAX variants in exon 4 →](https://dantelabs.com/genes/max/variants?exon=4) [MAX's gene diagram →](https://dantelabs.com/genes/max#gene-structure) ## Molecular details | Gene | [MAX](https://dantelabs.com/genes/max) | | --------------------------- | ----------------------------------------------------------------------------------------------------------------------------------------------- | | Transcript | NM_002382.5 MANE Select | | Coding DNA change (HGVS c.) | c.200C>A | | Protein change (HGVS p.) | p.Ala67Asp p.A67D | | Predicted consequence | Missense [missense_variant (opens in a new tab)](https://purl.obolibrary.org/obo/SO_0001583) | | Predicted impact | Moderate | | Position (GRCh38) | chr14:65078008 G>T | | Position (GRCh37) | chr14:65544726 G>T | | dbSNP ID | [rs786202340 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/snp/rs786202340) | | ClinVar Variation ID | [VCV000185646 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/clinvar/variation/185646/) | | ClinVar Allele ID | 184110 | | ClinGen Allele Registry ID | [CA192517 (opens in a new tab)](https://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_canonicalid?canonicalid=CA192517) | | ClinVar name | NM_002382.5(MAX):c.200C>A (p.Ala67Asp) | ## MAX A67D in other databases - [ClinVar VCV000185646 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/clinvar/variation/185646/) - [dbSNP rs786202340 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/snp/rs786202340) - [ClinGen Allele Registry CA192517 (opens in a new tab)](https://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_canonicalid?canonicalid=CA192517) - [gnomAD 14-65078008-G-T (opens in a new tab)](https://gnomad.broadinstitute.org/variant/14-65078008-G-T?dataset=gnomad_r4) - [Ensembl rs786202340 (opens in a new tab)](https://www.ensembl.org/Homo_sapiens/Variation/Explore?v=rs786202340) ## Reports that look at this variant (1) These Genome Test condition reports include A67D among the variants they look at. | Report | Conditions | Inheritance | | --------------------------------------------------------------------------------------------------------------------------- | ----------------------------------------- | ------------------ | | [Hereditary Pheochromocytoma and Paraganglioma](https://dantelabs.com/conditions/hereditary-pheochromocytoma-paraganglioma) | Hereditary pheochromocytoma-paraganglioma | Autosomal dominant | ## Other variants in MAX - [R33X Pathogenic 2 stars out of 4](https://dantelabs.com/genes/max/variants/r33x) [All MAX variants](https://dantelabs.com/genes/max/variants) ## Limitations This page describes publicly available information about a genetic variant. It is not a diagnosis, and it says nothing about whether you or anyone else carries this variant. Classifications come from ClinVar and change as new evidence is reviewed. A classification here may differ from the one in ClinVar today, or from the one a laboratory reports. Whole genome sequencing with short reads can miss or miscall some variants, particularly in repeated or highly similar stretches of DNA and in large insertions, deletions or rearrangements. If you have questions about a variant in your own results or in your family, talk to a genetic counsellor or your doctor. ## Sources & credits - Classifications from ClinVar (release 2026-10-12), National Center for Biotechnology Information. - Condition terms from the Mondo Disease Ontology (release 2026-10-06), used under CC BY 4.0. - Gene symbols and names from the HUGO Gene Nomenclature Committee (release 2026-10-16). - Allele identifiers from the ClinGen Allele Registry (release 2026-10-16-c4908f54). - Reference SNP identifiers from dbSNP (release b157), National Center for Biotechnology Information. - Gene–disease links from the Gene Curation Coalition, GenCC (release 2026-10-16). - Difficult regions from the Genome in a Bottle Consortium (release v3.6). - Transcripts from MANE (release v1.5), NCBI and EMBL-EBI. - Predicted consequences from mehari (release 0.11.0), with transcript models from cdot. - Built from Dante Labs data release 2026.10.16-c6eea6bf of 16 October 2026. ## Cite this page APA > Dante Labs. (16 October 2026). MAX A67D (c.200C>A, rs786202340) (Version 2026.10.16-c6eea6bf). Retrieved 17 October 2026, from https\://dantelabs.com/genes/max/variants/a67d Vancouver > Dante Labs. MAX A67D (c.200C>A, rs786202340) \[Internet]. Version 2026.10.16-c6eea6bf. 16 October 2026 \[cited 17 October 2026]. Available from: https\://dantelabs.com/genes/max/variants/a67d Download citation [RIS](https://dantelabs.com/genes/max/variants/a67d/cite.ris) [BibTeX](https://dantelabs.com/genes/max/variants/a67d/cite.bib) [CSL-JSON](https://dantelabs.com/genes/max/variants/a67d/cite.json) ## Read your whole genome From $449 Free shipping · Results in 6–8 weeks [Explore the Genome Test](https://dantelabs.com/whole-genome-sequencing)