Original source

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

Alleles
-/T
Location

Chromosome 3: between 128781258 and 128781259 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.128781258_128781259insT

Variation displays