Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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