Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 7 HGVS names - click the plus to show

About this variant

Variant displays