Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 1:2228865 (forward strand) | View in location tab

Co-located

with COSMIC COSM3689349 (C/G)

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Variation displays