Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.33 (G)
Location

Chromosome 12:52287653 (forward strand) | View in location tab

Co-located

with COSMIC COSM147519 (A/G)

Most severe consequence
Evidence status

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

Variation displays