Original source

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

Alleles
-/T
Location

Chromosome 3: between 129062415 and 129062416 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.129062415_129062416insT

Variation displays