Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.17 (C)
Location

Chromosome 3:137083096 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs60294884

HGVS name

3:g.137083096A>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant has 3449 sample genotypes and is mentioned in 5 citations.

Variant displays