Original source

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

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

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