Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)
Location

Chromosome 12:109814742 (forward strand) | View in location tab

Co-located

with COSMIC COSM4146536 (G/A) ; HGMD-PUBLIC CM094852

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 19 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni1-Quad, Illumina_ExomeChip

About this variant

This variant overlaps 9 transcripts, has 2807 individual genotypes, is associated with 3 phenotypes and is mentioned in 3 citations.

Variation displays