Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance


Archive dbSNP rs17849091

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts, has 1202 individual genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variation displays