Original source

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

C/A | Ancestral: C | Ambiguity code: M | MAF: 0.20 (C)

Chromosome 1:192567683 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs60598391, rs12734298

HGVS name


This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 3764 sample genotypes, is associated with 2 phenotypes and is mentioned in 18 citations.

Variant displays