Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.18 (C)
Location

Chromosome 13:26957130 (forward strand)|View in location tab

Most severe consequence
 
Regulatory region variant
Evidence status

Synonyms

Archive dbSNP rs60996343

HGVS name

13:g.26957130T>C

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 4030 sample genotypes, is associated with 4 phenotypes and is mentioned in 8 citations.

Variant displays