Original source

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

This variant has 4 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

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

Variant displays