Original source

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

Alleles
-/A | MAF: 0.01 (A)
Location

Chromosome 11: between 34458828 and 34458829 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.34458828_34458829insA

Variation displays