Original source

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

T/A | Ancestral: T | Ambiguity code: W

Chromosome 12:7692051 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs9300241, rs58181608

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays