Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519436
rs1057519436
DHX30
0.882 0.200 3 47846550 missense variant G/A snv
CUI: C0036572
Disease: Seizures
Seizures 		0.700 0