Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 10:89720907 (forward strand) | View in location tab

Co-located

with COSMIC COSM5914 (G/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17849091

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays