Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.41 (C)
Location

Chromosome 12:109805275 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57015251

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2510 individual genotypes.

Variation displays