Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:201328371 (forward strand) | View in location tab

Co-located

with COSMIC COSM209474 (G/A)

Most severe consequence
Evidence status

This variation has 15 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays