Original source

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

Alleles
-/TGTGTGTGT
Location

Chromosome 20: between 46709259 and 46709260 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

20:g.46709259_46709260insTGTGTGTGT

Variation displays