Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.27 (C)
Location

Chromosome 13:27665803 (forward strand) | View in location tab

Co-located

with COSMIC COSM147655 (G/C)

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays