Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 17:27765605 (forward strand) | View in location tab

Co-located

with COSMIC COSM4000072 (A/G)

Most severe consequence
Evidence status

Synonyms

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays