Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.03 (C)

Chromosome 10:37952139 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


This variant has 5 synonyms - Show

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3274 sample genotypes and is mentioned in 1 citation.

Variant displays