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: rs6017317
rs6017317 		1.000 0.080 20 44318326 intergenic variant T/G snv 0.30
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 0.667 2 2011 2017
dbSNP: rs6812193
rs6812193
FAM47E ; FAM47E-STBD1 ; LOC105377286
0.882 0.080 4 76277833 intron variant C/T snv 0.38
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.880 0.667 2 2009 2017
dbSNP: rs7805747
rs7805747
PRKAG2
1.000 0.080 7 151710715 intron variant G/A snv 0.26
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.710 0.667 2 2010 2018
dbSNP: rs995030
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis 		0.710 0.667 2 2009 2016
dbSNP: rs10260404
rs10260404
DPP6
0.925 0.080 7 154513713 intron variant T/C snv 0.35
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.820 0.667 1 2008 2011
dbSNP: rs10273639
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv
CUI: C0030305
Disease: Pancreatitis
Pancreatitis 		0.820 0.667 1 2012 2020
dbSNP: rs10913469
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22
CUI: C0028754
Disease: Obesity
Obesity 		0.720 0.667 1 2009 2013
dbSNP: rs10915437
rs10915437 		1.000 0.040 1 4122946 intergenic variant A/G snv 0.29
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.820 0.667 1 2013 2017
dbSNP: rs115550680
rs115550680
ABCA7
1.000 0.080 19 1050421 intron variant A/G snv 1.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.830 0.667 1 2013 2019
dbSNP: rs11568818
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.720 0.667 1 2013 2018
dbSNP: rs11747270
rs11747270
IRGM
0.790 0.240 5 150879305 intron variant A/G snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.820 0.667 1 2008 2020
dbSNP: rs11754661
rs11754661
MTHFD1L
0.851 0.120 6 150885942 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.820 0.667 1 2010 2011
dbSNP: rs12807809
rs12807809 		0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.720 0.667 1 2014 2017
dbSNP: rs12966547
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 0.667 1 2011 2019
dbSNP: rs13254738
rs13254738
PCAT1 ; PRNCR1 ; CASC19
0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.720 0.667 1 2008 2012
dbSNP: rs1333040
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.720 0.667 1 2007 2011
dbSNP: rs138880
rs138880
BRD1
1.000 0.040 22 49824963 intron variant A/C snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.820 0.667 1 2010 2017
dbSNP: rs1465618
rs1465618
THADA
0.882 0.160 2 43326810 intron variant T/C snv 0.80
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.720 0.667 1 2009 2016
dbSNP: rs1713985
rs1713985
REST
0.882 0.040 4 56920284 intron variant G/T snv 0.92
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.820 0.667 1 2011 2013
dbSNP: rs17632542
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.750 0.667 1 2011 2015
dbSNP: rs1800630
rs1800630
LTA ; TNF ; LOC100287329
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.720 0.667 1 2011 2019
dbSNP: rs1999930
rs1999930
FRK
0.882 0.040 6 116065971 intergenic variant C/A;G;T snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.820 0.667 1 2011 2018
dbSNP: rs2228603
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.720 0.667 1 2011 2016
dbSNP: rs224136
rs224136 		0.925 0.120 10 62710915 intron variant C/A;T snv 0.34
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 0.667 1 2007 2019
dbSNP: rs2373000
rs2373000
QPCT
1.000 0.040 2 37365485 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.820 0.667 1 2013 2016