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: rs2071277
rs2071277
NOTCH4
0.882 0.200 6 32203906 intron variant T/C snv 0.48 0.46
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.810 1.000 1 2012 2012
dbSNP: rs3131296
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 0.667 1 2009 2014
dbSNP: rs404860
rs404860
NOTCH4
0.925 0.160 6 32216568 non coding transcript exon variant T/C snv 0.21
CUI: C0004096
Disease: Asthma
Asthma 		0.810 1.000 1 2011 2011
dbSNP: rs2071278
rs2071278
NOTCH4
1.000 0.120 6 32197667 intron variant A/G snv 0.13
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.800 1.000 1 2012 2012
dbSNP: rs3132935
rs3132935
NOTCH4
0.925 0.160 6 32203298 non coding transcript exon variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2013
dbSNP: rs3134931
rs3134931
NOTCH4
6 32222843 intron variant T/C snv 0.35 0.37
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement 		0.800 1.000 1 2013 2013
dbSNP: rs443198
rs443198
NOTCH4
0.851 0.200 6 32222629 synonymous variant A/G snv 0.38 0.39
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.800 1.000 1 2010 2011
dbSNP: rs115344853
rs115344853
NOTCH4
1.000 0.040 6 32197667 intron variant A/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs3096702
rs3096702
NOTCH4
0.925 0.080 6 32224554 upstream gene variant A/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 2 2013 2018
dbSNP: rs115344853
rs115344853
NOTCH4
1.000 0.040 6 32197667 intron variant A/G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs115695709
rs115695709
NOTCH4
6 32223562 intron variant C/T snv
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs115963308
rs115963308
NOTCH4
1.000 0.040 6 32223264 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs115963308
rs115963308
NOTCH4
1.000 0.040 6 32223264 intron variant G/A;C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs138753323
rs138753323
NOTCH4
1.000 0.040 6 32205822 intron variant T/C snv 1.8E-02
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
dbSNP: rs147499485
rs147499485
NOTCH4
6 32216247 non coding transcript exon variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs16869834
rs16869834
NOTCH4
6 32211932 intron variant A/G snv 5.5E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2071286
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.700 1.000 1 2014 2014
dbSNP: rs2071286
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17
CUI: C0010403
Disease: Cryoglobulinemia
Cryoglobulinemia 		0.700 1.000 1 2014 2014
dbSNP: rs3132947
rs3132947
NOTCH4
1.000 0.120 6 32209005 intron variant G/T snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3132947
rs3132947
NOTCH4
1.000 0.120 6 32209005 intron variant G/T snv 0.19
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2019 2019
dbSNP: rs35565902
rs35565902
NOTCH4
6 32222211 intron variant TCT/- delins 0.26
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs3830041
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs3830041
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs3830041
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs3830041
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019