Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.30 (G)
Location

Chromosome 10:52773037 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60942321

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, has 2868 sample genotypes and is mentioned in 2 citations.

Variant displays