Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome 12:52287624 (forward strand) | View in location tab

Co-located

with COSMIC COSM4042813 (G/A)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs75304109

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts and has 1 individual genotype.

Variation displays