Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.37 (C)

Chromosome 10:87966988 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs17346569, rs3193466

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 4164 sample genotypes and is mentioned in 9 citations.

Variant displays