Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60996343

HGVS name

13:g.26957130T>C

This variation has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 4030 individual genotypes, is associated with 4 phenotypes and is mentioned in 8 citations.

Variation displays