Variant
VWF H1536_V1537del
NM_000552.5(VWF):c.4606_4611del (p.His1536_Val1537del)
- p.His1536_Val1537del
- p.H1536_V1537del
- rs2136412203
- ClinVar classification
- Likely pathogenic
- Review status
- 3 stars out of 4reviewed by expert panel
- Last evaluated
- 6 May 2025
- Expert panel
- ClinGen von Willebrand Disease Variant Curation Expert Panel, ClinGen
Data current to ClinVar release 2026-10-12 · Dante Labs data release 2026.10.16-c6eea6bfFacts last changed 16 October 2026
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Summary
H1536_V1537del is an in-frame variant in VWF: it adds or removes one or more amino acids without shifting how the rest of the gene's code is read. ClinVar classifies it as likely pathogenic for von Willebrand disease type 2A (reviewed by expert panel).
ClinVar classifications
| Condition | Classification | Review status | Submissions | Last evaluated |
|---|---|---|---|---|
| von Willebrand disease type 2AClinVar VCV001684012 (opens in a new tab) | Likely pathogenic | 3 stars out of 4reviewed by expert panel | 1 submission | 6 May 2025 |
Classifications as ClinVar records them in release 2026-10-12. ClinVar updates them as evidence is reviewed.
Where it lies in VWF
H1536_V1537del lies in exon 28 of the 52 in VWF's MANE Select transcript, NM_000552.5.
Molecular details
| Gene | VWF |
|---|---|
| Transcript | NM_000552.5MANE Select |
| Coding DNA change (HGVS c.) | c.4606_4611del |
| Protein change (HGVS p.) | p.His1536_Val1537delp.H1536_V1537del |
| Predicted consequence | In-frame insertion or deletionconservative_inframe_deletion (opens in a new tab) |
| Predicted impact | Moderate |
| Position (GRCh38) | chr12:6018806 TGACGTG>T |
| Position (GRCh37) | chr12:6127972 TGACGTG>T |
| dbSNP ID | rs2136412203 (opens in a new tab) |
| ClinVar Variation ID | VCV001684012 (opens in a new tab) |
| ClinVar Allele ID | 1675943 |
| ClinGen Allele Registry ID | CA2573148473 (opens in a new tab) |
| ClinVar name | NM_000552.5(VWF):c.4606_4611del (p.His1536_Val1537del) |
VWF H1536_V1537del in other databases
Reports that look at this variant (1)
These Genome Test condition reports include H1536_V1537del among the variants they look at.
| Report | Conditions | Inheritance |
|---|---|---|
| Hereditary Von Willebrand Disease | Hereditary Von Willebrand Disease |
Other variants in VWF
- c.4885G>CPathogenic3 stars out of 4
- C804FLikely pathogenic3 stars out of 4
- C849YLikely pathogenic3 stars out of 4
- C1060RPathogenic3 stars out of 4
- C1149RPathogenic3 stars out of 4
- C1190FLikely pathogenic3 stars out of 4
- C1190RPathogenic3 stars out of 4
- C1190YPathogenic3 stars out of 4
- C2773RPathogenic3 stars out of 4
- C2773SPathogenic3 stars out of 4
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
Dante Labs. (16 October 2026). VWF H1536_V1537del (c.4606_4611del, rs2136412203) (Version 2026.10.16-c6eea6bf). Retrieved 16 October 2026, from https://dantelabs.com/genes/vwf/variants/h1536-v1537del
Dante Labs. VWF H1536_V1537del (c.4606_4611del, rs2136412203) [Internet]. Version 2026.10.16-c6eea6bf. 16 October 2026 [cited 16 October 2026]. Available from: https://dantelabs.com/genes/vwf/variants/h1536-v1537del
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