VSTM2A-OT1

Chr 7

VSTM2A overlapping transcript 1

Also known as: GS1-18A18.1

NCBI Gene: 285878ENSG00000224223
8
ClinVar variants
5
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— VSTM2A-OT1
📋
ClinVar Variants
5 Pathogenic / Likely Pathogenic· 3 VUS of 8 total submissions
Some data sources returned errors (1)

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

8 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic4
Likely Pathogenic1
VUS3
4
Pathogenic
1
Likely Pathogenic
3
VUS

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————4
Likely Pathogenic
————1
VUS
————3
Likely Benign
————0
Benign
————0
Total—8

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

VSTM2A-OT1 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

No publications found for VSTM2A-OT1

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools