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 2:232538993 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.232538993G>A

Variation displays