Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 18: between 5392252 and 5392253 (forward strand) | View in location tab

Most severe consequence
HGVS name

18:g.5392252_5392253insT

Variation displays