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: 0.43 (A)
Location

Chromosome 11:18264546 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.18264546A>G

Variation displays