Original source

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

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

Chromosome 2: between 113587327 and 113587328 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.113587327_113587328insT

Variation displays