Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.01 (-)
Location

Chromosome 22:37125606 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.37125606delC

Variation displays