Original source

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

Alleles
-/G
Location

Chromosome 7: between 100769706 and 100769707 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.100769706_100769707insG

Variation displays