SNIP1, Smad nuclear interacting protein 1, 79753

N. diseases: 45; N. variants: 2
Disease: Epilepsy, Rolandic ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs202020647
rs202020647 		1.000 0.040 1 37540752 missense variant G/A snv 1.8E-04 1.3E-04
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		Nervous System Diseases 0.700 1.000 1 2018 2018