Original source

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

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

Chromosome 11: between 34437281 and 34437282 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.34437281_34437282insA

Variation displays