Original source

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

Alleles
-/T
Location

Chromosome 6: between 34394684 and 34394685 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.34394684_34394685insT

Variation displays