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: rs1016342
rs1016342
1.000 0.080 8 127080210 non coding transcript exon variant C/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.700 1.000 1 2007 2007
dbSNP: rs1031588
rs1031588
1.000 0.080 8 127081032 non coding transcript exon variant C/A snv 0.24
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.700 1.000 1 2007 2007
dbSNP: rs1042602
rs1042602
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24
CUI: C0025209
Disease: Melanosis
Melanosis
0.700 1.000 1 2007 2007
dbSNP: rs10485165
rs10485165
6 88403098 intron variant C/G;T snv
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0.700 1.000 1 2007 2007
dbSNP: rs10485165
rs10485165
6 88403098 intron variant C/G;T snv
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement
0.700 1.000 1 2007 2007
dbSNP: rs10496262
rs10496262
2 81524000 intergenic variant C/A snv 0.12
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.800 1.000 1 2007 2007
dbSNP: rs10496265
rs10496265
2 81441684 intergenic variant T/C snv 0.12
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.800 1.000 1 2007 2007
dbSNP: rs10497721
rs10497721
1.000 0.040 2 192049636 intron variant C/A;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2007 2007
dbSNP: rs10497721
rs10497721
1.000 0.040 2 192049636 intron variant C/A;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2007 2007
dbSNP: rs10498345
rs10498345
1.000 0.040 14 38551301 intergenic variant T/A snv 6.4E-02
CUI: C0010073
Disease: Coronary Artery Vasospasm
Coronary Artery Vasospasm
0.810 1.000 1 2007 2007
dbSNP: rs10506701
rs10506701
12 74192430 intron variant T/G snv 0.15
CUI: C0005938
Disease: Bone Density
Bone Density
0.700 1.000 1 2007 2007
dbSNP: rs10518765
rs10518765
1.000 0.040 15 54388434 intron variant A/C snv 0.16
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement
0.700 1.000 1 2007 2007
dbSNP: rs10789230
rs10789230
1.000 0.040 1 67264945 downstream gene variant G/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs10801047
rs10801047
1.000 0.040 1 191590226 intergenic variant A/T snv 0.82
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs11052552
rs11052552
1.000 0.120 12 9703362 upstream gene variant T/G snv 0.42
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2007 2007
dbSNP: rs1106683
rs1106683
7 131768766 intergenic variant G/A snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2007 2007
dbSNP: rs1119582
rs1119582
5 125907327 intron variant T/C snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.700 1.000 1 2007 2007
dbSNP: rs11209002
rs11209002
1.000 0.040 1 67124778 intron variant T/C snv 0.77
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs11209003
rs11209003
1.000 0.040 1 67135449 intron variant G/T snv 0.28
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs11465802
rs11465802
1.000 0.040 1 67219915 intron variant A/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs1154865
rs1154865
0.882 0.160 12 73596057 intergenic variant C/G snv 0.22
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.700 1.000 1 2007 2007
dbSNP: rs1158167
rs1158167
20 23597552 downstream gene variant G/A snv 0.72
CUI: C1619716
Disease: Cystatin C measurement
Cystatin C measurement
0.800 1.000 1 2007 2007
dbSNP: rs1160297
rs1160297
2 53010182 intergenic variant G/C snv 0.69
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2007 2007
dbSNP: rs12035082
rs12035082
1.000 0.040 1 172929237 intron variant T/C snv 0.52
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007
dbSNP: rs12567232
rs12567232
1.000 0.040 1 67262335 downstream gene variant G/A snv 0.27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2007 2007