Original source

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

Alleles
G/- | Ancestral: G
Location

Chromosome 16:23181011 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.23181011delG

Variation displays