Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.10 (G)
Location

Chromosome 4:3518035 (forward strand) | View in location tab

Co-located

with COSMIC COSM4159037 (A/G)

Most severe consequence
Evidence status

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts and has 2537 individual genotypes.

Variation displays