Original source

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

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

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


with COSMIC COSM5914 (G/T)

Most severe consequence
3 prime UTR variant
Evidence status

Clinical significance


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