Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57552079, rs17338574

HGVS name

7:g.128954129T>C

This variation has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 3613 individual genotypes, is associated with 11 phenotypes and is mentioned in 62 citations.

Variation displays