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 2:236166256 (forward strand) | View in location tab

Co-located

with COSMIC COSM1253122 (G/A)

Most severe consequence

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

Variation displays