Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ambiguity code: R | MAF: 0.27 (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

About this variant

This variant overlaps 2 transcripts, has 2605 individual genotypes and is mentioned in 2 citations.

Variation displays