Original source

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

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

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

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