Original source

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

Alleles
-/T
Location

Chromosome 7: between 100718932 and 100718933 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.100718932_100718933insT

Variation displays