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: rs1343151
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2006 2007
dbSNP: rs1373692
rs1373692 		1.000 0.040 5 40431081 non coding transcript exon variant A/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
dbSNP: rs1378897
rs1378897
PCAT1 ; CASC19
0.925 0.080 8 127110414 intron variant C/T snv 5.7E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1379659
rs1379659
SLIT2
4 20619060 3 prime UTR variant G/A snv 0.85 0.86
CUI: C0011904
Disease: Diagnostic Techniques, Cardiovascular
Diagnostic Techniques, Cardiovascular 		0.700 1.000 1 2007 2007
dbSNP: rs1379659
rs1379659
SLIT2
4 20619060 3 prime UTR variant G/A snv 0.85 0.86
CUI: C0080310
Disease: Left Ventricular Function
Left Ventricular Function 		0.700 1.000 1 2007 2007
dbSNP: rs1397048
rs1397048
OR9G1
11 56698623 upstream gene variant C/T snv 0.54
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2007 2007
dbSNP: rs1456305
rs1456305
PCAT1 ; CASC19
1.000 0.080 8 127115007 intron variant G/A snv 0.88
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1456306
rs1456306
PCAT1 ; CASC19
0.925 0.080 8 127104255 intron variant G/A snv 0.23
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1456314
rs1456314
PCAT1
1.000 0.080 8 127063445 intron variant A/G snv 0.64
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1540771
rs1540771
LOC105374875
1.000 0.040 6 466033 intron variant C/A;T snv
CUI: C0025209
Disease: Melanosis
Melanosis 		0.700 1.000 1 2007 2007
dbSNP: rs1551510
rs1551510
PCAT1 ; PRNCR1 ; CASC19 ; PCAT2
1.000 0.080 8 127081233 non coding transcript exon variant C/T snv 0.56
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1667394
rs1667394
HERC2
15 28285036 intron variant C/A;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.800 1.000 1 2007 2007
dbSNP: rs17532515
rs17532515
MGAT4D
4 140466284 intron variant C/T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2007 2007
dbSNP: rs17831626
rs17831626
PCAT1
1.000 0.080 8 127068178 intron variant G/T snv 0.31
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1823068
rs1823068
PDE4D ; LOC107986348
5 59380223 intron variant A/G snv 0.15
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2007 2007
dbSNP: rs1834640
rs1834640 		15 48099968 intergenic variant A/G snv 0.29
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.800 1.000 1 2007 2007
dbSNP: rs1978503
rs1978503
LINC01416 ; LOC107985164
0.882 0.160 18 55997051 non coding transcript exon variant A/G snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2007 2007
dbSNP: rs1992660
rs1992660 		1.000 0.040 5 40414965 upstream gene variant C/T snv 0.58
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
dbSNP: rs1998303
rs1998303 		9 82800066 intergenic variant A/G snv 0.37
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2007 2007
dbSNP: rs1998303
rs1998303 		9 82800066 intergenic variant A/G snv 0.37
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2007 2007
dbSNP: rs2064689
rs2064689
IL23R ; C1orf141
1.000 0.040 1 67187327 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
dbSNP: rs2165468
rs2165468
LINC02669 ; LOC105376360
10 3473913 intron variant C/A snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2007 2007
dbSNP: rs2179965
rs2179965
PKN2-AS1
1 88336329 intron variant A/G snv 0.17
CUI: C0027902
Disease: Neuropsychological Tests
Neuropsychological Tests 		0.700 1.000 1 2007 2007
dbSNP: rs2387326
rs2387326 		10 128135192 intergenic variant C/T snv 0.24
CUI: C0042879
Disease: Vitamin K Assay
Vitamin K Assay 		0.700 1.000 1 2007 2007
dbSNP: rs2390582
rs2390582
LOC105378851
1 90478350 intergenic variant A/G snv 0.15
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.800 1.000 1 2007 2007