Original source

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

Alleles
-/T | MAF: 0.08 (T)
Location

Chromosome 18: between 5392251 and 5392252 (forward strand) | View in location tab

Most severe consequence
HGVS name

18:g.5392251_5392252insT

Variation displays