Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.21 (C)
Location

Chromosome 10:113029056 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17685444, rs60689663

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 15 transcripts, 2 regulatory features, has 3996 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays