Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.45 (T)

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


with HGMD-PUBLIC CR051714

Most severe consequence
Evidence status


Archive dbSNP rs3737956

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

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

About this variant

This variant overlaps 2 transcripts, has 1686 individual genotypes and is mentioned in 12 citations.

Variation displays