Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.07 (C)
Location

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

Co-located

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

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_033893

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

Genotyping chips

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

Variation displays