Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 7:100720172 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.100720172delA

Variation displays