Original source

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

Alleles
-/A | MAF: 0.02 (A)
Location

Chromosome 11: between 119055249 and 119055250 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.119055249_119055250insA

Variation displays