Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome 12:52287624 (forward strand) | View in location tab

Co-located

with dbSNP rs75304109 (A/G)

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

Variation displays