Original source

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

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

Chromosome 13:113295328-113295329 (forward strand) | View in location tab

Most severe consequence
HGVS name

13:g.113295328_113295329delTC

Variation displays