Original source

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

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

Chromosome 13:113295332-113295335 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.113295332_113295335delTCTT

Variation displays