Original source

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

Alleles
C/A|Ancestral: A|Ambiguity code: M|MAF: 0.14 (A)
Location

Chromosome 1:12164182 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

1:g.12164182C>A

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 3691 sample genotypes and is mentioned in 2 citations.

Variant displays