Source: ALL

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: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.040 1.000 4 2018 2020
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2020 2020
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.070 0.714 7 2009 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.070 0.714 7 2009 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.060 0.833 6 2010 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 1.000 4 2014 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 1.000 4 2012 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 1.000 4 2012 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.040 1.000 4 2010 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome
0.020 1.000 2 2017 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.020 0.500 2 2015 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.020 1.000 2 2015 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.020 1.000 2 2012 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2017 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.020 0.500 2 2014 2019
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 0.500 2 2018 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0028754
Disease: Obesity
Obesity
0.020 1.000 2 2014 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.020 1.000 2 2009 2019
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.020 0.500 2 2015 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis
0.720 1.000 2 2015 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0023980
Disease: Longevity
Longevity
0.700 1.000 2 2016 2019
dbSNP: rs1474348
rs1474348
0.882 0.080 7 22728289 intron variant C/G snv 0.71
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1524107
rs1524107
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2019 2019
dbSNP: rs1524107
rs1524107
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1554606
rs1554606
0.925 0.120 7 22729088 intron variant T/A;G snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 < 0.001 1 2019 2019