Original source

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

Alleles
TG/-
Location

Chromosome 19:48394182-48394183 (forward strand) | View in location tab

Most severe consequence
HGVS name

19:g.48394182_48394183delTG

Variation displays