Original source

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

Alleles
AG/- | MAF: 0.03 (-)
Location

Chromosome 13:113295270-113295271 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.113295270_113295271delAG

About this variant

This variant overlaps 1 transcript and has 1092 individual genotypes.

Variation displays