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: rs1912439
rs1912439
NOS1AP
1 162324355 intron variant A/G snv 0.98
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1912439
rs1912439
NOS1AP
1 162324355 intron variant A/G snv 0.98
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2661814
rs2661814
NOS1AP
1 162350216 intron variant G/A snv 0.95
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2661814
rs2661814
NOS1AP
1 162350216 intron variant G/A snv 0.95
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2819325
rs2819325
NOS1AP
1 162313721 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2819325
rs2819325
NOS1AP
1 162313721 intron variant G/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2819325
rs2819325
NOS1AP
1 162313721 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370911
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370911
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370911
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370911
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370911
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370911
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs425820
rs425820
NOS1AP
1 162323874 intron variant G/A snv 0.98
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs425820
rs425820
NOS1AP
1 162323874 intron variant G/A snv 0.98
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4306106
rs4306106
NOS1AP
1 162202204 intron variant G/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4391647
rs4391647
NOS1AP
1 162217141 intron variant A/G snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4480335
rs4480335
NOS1AP
1 162203587 intron variant A/C snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4657173
rs4657173
NOS1AP
1 162215756 intron variant G/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs4657175
rs4657175
NOS1AP
1.000 0.040 1 162225948 intron variant T/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2012 2012
dbSNP: rs6664702
rs6664702
NOS1AP
1 162235117 intron variant T/C snv 0.32
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs6667431
rs6667431
NOS1AP
1 162198131 intron variant G/A snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs6692381
rs6692381
NOS1AP
1 162198094 intron variant C/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs7534004
rs7534004
NOS1AP ; LOC105371475
1 162176919 intron variant G/A snv 0.21
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs12029454
rs12029454
NOS1AP ; LOC105371475
1 162163327 intron variant G/A snv 0.21
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 2 2009 2019