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: 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: 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: 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: rs11805598
rs11805598
NOS1AP ; LOC105371475
1 162170546 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs12135795
rs12135795
NOS1AP
1 162179975 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs12724220
rs12724220
NOS1AP
1 162183208 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
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: 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: 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: rs6671817
rs6671817
NOS1AP
1 162183436 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs7549718
rs7549718
NOS1AP ; LOC105371475
1 162171072 intron variant A/G snv 0.44
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs4657178
rs4657178
NOS1AP
1 162240820 intron variant C/A;G;T snv 0.31
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.800 1.000 1 2009 2019
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: 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: rs1932932
rs1932932
NOS1AP ; LOC105371475
1 162150789 intron variant C/G snv 0.45
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs10919021
rs10919021
NOS1AP
1 162265600 intron variant C/T snv 0.97
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12123267
rs12123267
NOS1AP
1 162229561 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: rs12734991
rs12734991
NOS1AP
1 162224786 intron variant C/T snv 0.41
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
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