Source: GWASDB

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: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 0.667 2 2009 2014
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 3 2007 2011
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis 		0.700 1.000 1 2012 2012
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2014 2014
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2007 2007
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2010 2010