Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.09 (C)
Location

Chromosome 12:21657573 (forward strand)|View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs16924185, rs187631

HGVS names

This variant has 7 HGVS names - Show

About this variant

Variant displays