Original source

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

This variant has assays on 11 chips - click the plus to show

About this variant

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

Variant displays