Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60598391, rs12734298

HGVS name

1:g.192567683C>A

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