Original source

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

Alleles
C/G|Ambiguity code: S|MAF: 0.42 (G)
Location

Chromosome 12:52286153 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2854 sample genotypes and is mentioned in 3 citations.

Variant displays