Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 22:37125504 (forward strand) | View in location tab

Most severe consequence
HGVS name

22:g.37125504delA

Variation displays