Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.15 (C)
Location

Chromosome 2:43623451 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61359010

HGVS name

2:g.43623451T>C

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 1 transcript, has 3603 sample genotypes and is mentioned in 2 citations.

Variant displays