Original source

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

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

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

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57525489

HGVS name

14:g.53944201T>C

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2512 sample genotypes, is associated with 1 phenotype and is mentioned in 56 citations.

Variant displays