Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.43 (G)
Location

Chromosome 10:87961150 (forward strand)|View in location tab

Co-located variant

COSMIC COSM5914

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs17849091

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2606 sample genotypes, is associated with 1 phenotype and is mentioned in 7 citations.

Variant displays