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: rs4657175
rs4657175
NOS1AP
1.000 0.040 1 162225948 intron variant T/C;G snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 2 2012 2019
dbSNP: rs10127719
rs10127719
NOS1AP
1 162186380 intron variant T/A;C snv
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10918796
rs10918796
NOS1AP ; LOC105371475
1 162163553 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
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: rs4656355
rs4656355
NOS1AP ; LOC105371475
1 162154007 intron variant A/C;G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
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: rs16860953
rs16860953
NOS1AP
1 162364127 5 prime UTR variant G/A snv 2.1E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16860953
rs16860953
NOS1AP
1 162364127 5 prime UTR variant G/A snv 2.1E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1510291
rs1510291
NOS1AP
1 162358271 intron variant C/T snv 3.5E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1510291
rs1510291
NOS1AP
1 162358271 intron variant C/T snv 3.5E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16857031
rs16857031
NOS1AP ; LOC105371475
1 162143120 intron variant C/G snv 0.18
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 1 2009 2019
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
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: rs10918602
rs10918602
NOS1AP
1 162067910 upstream gene variant T/C snv 0.25
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2012 2012
dbSNP: rs10800352
rs10800352
NOS1AP
1 162202899 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: 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: rs12116744
rs12116744
NOS1AP
1 162210666 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: rs12027785
rs12027785
NOS1AP
1 162211355 intron variant T/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: rs3934467
rs3934467
NOS1AP
1 162212887 intron variant C/T snv 0.27
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 1 2012 2019
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: rs12567315
rs12567315
NOS1AP
1 162196856 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