Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs17861105, rs60381661

HGVS name

15:g.74727108C>T

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

About this variant

This variant overlaps 10 transcripts, has 3362 individual genotypes, is associated with 2 phenotypes and is mentioned in 12 citations.

Variation displays