Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.01 (C)

Chromosome 15:43196904 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3179736, rs3203395, rs3924114

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and has 2771 sample genotypes.

Variant displays