Original source

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

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

Chromosome 11: between 119184540 and 119184541 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.119184540_119184541insA

Variation displays