Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.40 (C)
Location

Chromosome 1:153261225 (forward strand) | View in location tab

Co-located

with COSMIC COSM3747559 (A/C)

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 3 transcripts and has 3614 individual genotypes.

Variation displays