Original source

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

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

Chromosome 13:113949647-113949650 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.113949647_113949650delTCTT

Variation displays