Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (A)
Location

Chromosome 9:127912633 (forward strand) | View in location tab

Co-located

with COSMIC COSM3685503 (G/A)

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays