Original source

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

Alleles
-/G
Location

Chromosome 7: between 101126425 and 101126426 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.101126425_101126426insG

Variation displays