Source: GWASCAT

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: rs4821544
rs4821544
NCF4 ; NCF4-AS1
0.925 0.040 22 36862461 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.720 1.000 1 2008 2017
dbSNP: rs4821544
rs4821544
NCF4 ; NCF4-AS1
0.925 0.040 22 36862461 intron variant T/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4821544
rs4821544
NCF4 ; NCF4-AS1
0.925 0.040 22 36862461 intron variant T/A;C snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs4821544
rs4821544
NCF4 ; NCF4-AS1
0.925 0.040 22 36862461 intron variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2019 2019
dbSNP: rs760517
rs760517
NCF4 ; NCF4-AS1
22 36862944 intron variant C/T snv 0.42
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019