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: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0038354
Disease: Stomach Diseases
Stomach Diseases
0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2069837
rs2069837
0.724 0.520 7 22728408 intron variant A/C;G snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.010 1.000 1 2019 2019
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2019 2019
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2019 2019
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2019 2019
dbSNP: rs2069840
rs2069840
0.742 0.360 7 22728953 intron variant C/G snv 0.27
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.010 < 0.001 1 2019 2019
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2019 2019
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.010 1.000 1 2019 2019
dbSNP: rs2069845
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2069849
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2019 2019
dbSNP: rs2069849
rs2069849
IL6
0.882 0.120 7 22731537 missense variant C/G;T snv 4.4E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 1.000 1 2019 2019
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2019 2019
dbSNP: rs777906302
rs777906302
0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06
CUI: C0042029
Disease: Urinary tract infection
Urinary tract infection
0.010 1.000 1 2019 2019
dbSNP: rs777906302
rs777906302
0.925 0.160 7 22728782 synonymous variant A/G;T snv 4.0E-06
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
0.010 1.000 1 2019 2019
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: 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: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2018 2018
dbSNP: rs1800797
rs1800797
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
Congenital arteriovenous malformation
0.010 1.000 1 2018 2018