Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
TCTT/- | MAF: 0.02 (-)
Location

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

Most severe consequence
Evidence status

HGVS name

13:g.113295332_113295335delTCTT

About this variant

This variant overlaps 1 transcript and has 2504 individual genotypes.

Variation displays