Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.41 (T)

Chromosome 1:12207235 (forward strand) | View in location tab


with HGMD-PUBLIC CR051714

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3737956

This variant has 3 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 3086 sample genotypes and is mentioned in 12 citations.

Variant displays