Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.15 (C)
Location

Chromosome 20:45925376 (forward strand)|View in location tab

Most severe consequence
 
Regulatory region variant
Evidence status

Synonyms

Archive dbSNP rs59009182

HGVS name

20:g.45925376T>C

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 1 regulatory feature, has 3649 sample genotypes, is associated with 6 phenotypes and is mentioned in 7 citations.

Variant displays