Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.10 (C)

Chromosome 9:449874 (forward strand) | View in location tab


with COSMIC COSM3763951 (G/C), COSM3763950 (G/C)

Most severe consequence
Evidence status

Clinical significance


Uniprot VAR_033893

This variation has 13 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 13 transcripts, has 2549 individual genotypes and is associated with 1 phenotype.

Variation displays