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 14: between 28765569 and 28765570 (forward strand) | View in location tab

Most severe consequence
HGVS name

14:g.28765569_28765570insA

Variation displays