Original source

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

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

Chromosome 13: between 20531286 and 20531287 (forward strand) | View in location tab

Most severe consequence
HGVS name

13:g.20531286_20531287insT

Variation displays