Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome 16:23181649 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.23181649A>G

Variation displays