Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.07 (A)
Location

Chromosome 11:101583461 (forward strand) | View in location tab

Co-located

with COSMIC COSM3752082 (G/A)

Most severe consequence
Evidence status

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 7 transcripts, has 2505 individual genotypes and is mentioned in 4 citations.

Variation displays