Original source

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

Alleles
-/T
Location

Chromosome 6: between 34426907 and 34426908 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.34426907_34426908insT

Variation displays