Original source

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

Alleles
-/GGGGGGGGGG
Location

Chromosome 10: between 103989715 and 103989716 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.103989715_103989716insGGGGGGGGGG

Variation displays