Source: GWASCAT

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: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.820 1.000 3 2011 2017
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs11191560
rs11191560
NT5C2
10 103109281 intron variant T/C snv 8.4E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 3 2015 2018
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2017 2019
dbSNP: rs11191593
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 3 2011 2018
dbSNP: rs10786736
rs10786736
NT5C2 ; CNNM2
1.000 0.040 10 103089359 3 prime UTR variant G/C snv 9.9E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2014 2015
dbSNP: rs10883832
rs10883832
NT5C2
1.000 0.040 10 103111522 intron variant T/G snv 8.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs11191560
rs11191560
NT5C2
10 103109281 intron variant T/C snv 8.4E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2013 2013
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs11191580
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs11191582
rs11191582
NT5C2
1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs11191582
rs11191582
NT5C2
1.000 0.040 10 103153896 intron variant G/A snv 7.7E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs11191593
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs11191593
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs117208459
rs117208459
NT5C2
10 103126864 intron variant T/A snv 1.0E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs12219304
rs12219304
NT5C2
10 103171827 intron variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.700 1.000 1 2018 2018
dbSNP: rs12416331
rs12416331
NT5C2
1.000 0.040 10 103169157 intron variant T/A snv 8.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2018 2018
dbSNP: rs12416331
rs12416331
NT5C2
1.000 0.040 10 103169157 intron variant T/A snv 8.4E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs559546873
rs559546873
NT5C2
10 103186913 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 0.33
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs559546873
rs559546873
NT5C2
10 103186913 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 0.33
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016