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 13: between 19957146 and 19957147 (forward strand) | View in location tab

Most severe consequence
HGVS name

13:g.19957146_19957147insT

Variation displays