Original source

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

C/G | Ancestral: G | Ambiguity code: S | MAF: 0.04 (C)

Chromosome 12:21642695 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57897438, rs1677112

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2782 sample genotypes.

Variant displays