Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.06 (C)
Location

Chromosome 7:128954129 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57552079, rs17338574

HGVS name

7:g.128954129T>C

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3613 sample genotypes, is associated with 11 phenotypes and is mentioned in 66 citations.

Variant displays