Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.36 (A)
Location

Chromosome 16:23182544 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR014917

Most severe consequence
Evidence status

HGVS name

16:g.23182544A>G

Variation displays