Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.09 (T)
Location

Chromosome 15:74727108 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17861105, rs60381661

HGVS name

15:g.74727108C>T

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3362 sample genotypes, is associated with 3 phenotypes and is mentioned in 12 citations.

Variant displays