Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.43 (C)
Location

Chromosome 14:53944201 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57525489

HGVS name

14:g.53944201T>C

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

About this variant

This variant overlaps 2 transcripts, has 2512 individual genotypes, is associated with 1 phenotype and is mentioned in 49 citations.

Variation displays