Original source

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

Alleles
GT/-
Location

Chromosome 17:56592950-56592951 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.56592950_56592951delGT

Variation displays