Original source

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

This variant has 16 HGVS names - click the plus to show

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

About this variant

This variant overlaps 15 transcripts, 2 regulatory features, has 2890 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays