Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 16:23192915 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.23192915A>G

Variation displays