Source: CURATED

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: rs4795067
rs4795067
NOS2
0.882 0.280 17 27779649 intron variant A/G snv 0.31
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.820 1.000 3 2010 2015
dbSNP: rs28998802
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.810 1.000 2 2012 2016
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs28998800
rs28998800
NOS2
17 27799060 intron variant T/C snv 1.6E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs28998802
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs28998802
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs28998802
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs28998802
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs28998802
rs28998802
NOS2
0.807 0.120 17 27797882 intron variant G/A snv 0.11
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs7217335
rs7217335
NOS2
1.000 0.040 17 27771755 intron variant G/A snv 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2019 2019
dbSNP: rs8070472
rs8070472
NOS2
17 27774162 intron variant G/A snv 6.2E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8070472
rs8070472
NOS2
17 27774162 intron variant G/A snv 6.2E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9797244
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs9797244
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs9797244
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs9797244
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs9797244
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs9895831
rs9895831
NOS2
17 27762239 intron variant C/T snv 0.48
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs769900089
rs769900089
NOS2
1.000 0.080 17 27767837 missense variant C/A;T snv 4.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.700 0