Original source

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

Alleles
-/T
Location

Chromosome 1: between 27013731 and 27013732 (forward strand) | View in location tab

Most severe consequence
HGVS name

1:g.27013731dupT

Variation displays