Original source

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

Alleles
-/GGGGGGGGGG
Location

Chromosome 10: between 102229958 and 102229959 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.102229958_102229959insGGGGGGGGGG

Variation displays