Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:48920430 (forward strand) | View in location tab

Co-located

with COSMIC COSM3900501 (G/A)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_069163

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays