Source: ALL
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: rs114544105
rs114544105
6 32667852 intron variant G/A snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2017 2017
dbSNP: rs201043192
rs201043192
6 32660761 intron variant GG/- del
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs201184533
rs201184533
1.000 0.080 6 32665110 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2515895
rs2515895
1.000 0.040 6 32661183 intron variant T/C snv 0.24
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs281862010
rs281862010
6 32665113 intron variant C/A;G snv 1.5E-05
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2854277
rs2854277
6 32660307 intron variant C/T snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2018 2018
dbSNP: rs4988888
rs4988888
1.000 0.040 6 32667420 intron variant T/C snv 0.20
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs77296290
rs77296290
1.000 0.040 6 32667519 intron variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs9273542
rs9273542
6 32661035 intron variant C/A;T snv
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9273552
rs9273552
6 32661139 intron variant G/A snv 1.8E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9274477
rs9274477
0.925 0.080 6 32665936 intron variant A/G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs9274477
rs9274477
0.925 0.080 6 32665936 intron variant A/G snv
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs9274600
rs9274600
6 32667815 intron variant A/G snv 0.43
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
0.700 1.000 1 2015 2015
dbSNP: rs9274614
rs9274614
1.000 0.120 6 32668069 intron variant C/A;G snv
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs9274623
rs9274623
1.000 0.040 6 32668221 intron variant G/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs1130399
rs1130399
1.000 0.040 6 32661978 missense variant G/A;T snv 0.20
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs1140343
rs1140343
1.000 0.080 6 32661360 missense variant T/C;G snv 0.20 0.50
Steroid-sensitive nephrotic syndrome
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2015 2015
dbSNP: rs281862059
rs281862059
1.000 0.120 6 32665011 missense variant C/T snv 5.0E-06 7.6E-06
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs3189152
rs3189152
1.000 0.080 6 32666564 missense variant A/G;T snv 0.19 0.39
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
Digestive System Diseases; Infections 0.700 1.000 1 2013 2013
dbSNP: rs41563814
rs41563814
1.000 0.040 6 32664881 missense variant A/T snv 3.2E-05
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs9273643
rs9273643
0.925 0.120 6 32661407 missense variant A/G snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs9273643
rs9273643
0.925 0.120 6 32661407 missense variant A/G snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs9273643
rs9273643
0.925 0.120 6 32661407 missense variant A/G snv
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs9274390
rs9274390
0.925 0.080 6 32664882 missense variant C/G;T snv 3.9E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs9274390
rs9274390
0.925 0.080 6 32664882 missense variant C/G;T snv 3.9E-02
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.010 1.000 1 2016 2016