Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2227700
rs2227700
7 101138800 3 prime UTR variant T/C snp 1.1E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1 2012 2012
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0013537
Disease: Eclampsia
Eclampsia
Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2013 2013
dbSNP: rs763351020
rs763351020
0.724 0.464 7 101132046 missense variant C/T snp 4.0E-06
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Endocrine System Diseases; Female Urogenital Diseases and Pregnancy Complications; Neoplasms 0.020 1.000 2 2004 2009
dbSNP: rs763351020
rs763351020
0.724 0.464 7 101132046 missense variant C/T snp 4.0E-06
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.020 1.000 2 2008 2010
dbSNP: rs145850643
rs145850643
1.000 0.036 7 101135554 missense variant C/A,T snp 2.0E-05; 8.0E-06
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
Skin and Connective Tissue Diseases 0.010 1.000 1 2002 2002
dbSNP: rs1799768
rs1799768
0.923 0.143 7 101126425 TF binding site variant T/TA,TC,TG in-del 0.55
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1799768
rs1799768
0.923 0.143 7 101126425 TF binding site variant T/TA,TC,TG in-del 0.55
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Cardiovascular Diseases; Endocrine System Diseases; Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0029443
Disease: Osteomyelitis
Osteomyelitis
Bacterial Infections and Mycoses; Musculoskeletal Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Female Urogenital Diseases and Pregnancy Complications; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2011 2011
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0032962
Disease: Pregnancy Complications
Pregnancy Complications
Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2016 2016
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis
Endocrine System Diseases; Male Urogenital Diseases; Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
Malignant Testicular Germ Cell Tumor
0.010 1.000 1 2011 2011
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C1883486
Disease: Uterine Corpus Cancer
Uterine Corpus Cancer
0.010 1.000 1 2011 2011
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0025295
Disease: Meningitis, Pneumococcal
Meningitis, Pneumococcal
Bacterial Infections and Mycoses; Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1799889
rs1799889
0.734 0.321 7 101126430 intergenic variant A/G snp
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
Cardiovascular Diseases; Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2227631
rs2227631
0.923 0.071 7 101126257 intergenic variant A/G snp 0.53
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs2227631
rs2227631
0.923 0.071 7 101126257 intergenic variant A/G snp 0.53
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs2227667
rs2227667
0.923 0.179 7 101131468 intron variant A/G snp 0.23
5,10-Methylenetetrahydrofolate reductase deficiency
0.010 1.000 1 2015 2015
dbSNP: rs2227667
rs2227667
0.923 0.179 7 101131468 intron variant A/G snp 0.23
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
Cardiovascular Diseases; Hemic and Lymphatic Diseases; Immune System Diseases; Neoplasms 0.010 < 0.001 1 2015 2015
dbSNP: rs2227684
rs2227684
1.000 0.036 7 101133650 intron variant G/A,T snp 0.41 0.44
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs2227692
rs2227692
0.923 0.071 7 101135963 intron variant C/T snp 0.12
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2010 2010
dbSNP: rs2227692
rs2227692
0.923 0.071 7 101135963 intron variant C/T snp 0.12
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 < 0.001 1 2010 2010