Original source

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

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

Chromosome 2: between 112829750 and 112829751 (forward strand) | View in location tab

Most severe consequence
HGVS name

2:g.112829750_112829751insT

Variation displays