CREM, cAMP responsive element modulator, 1390

N. diseases: 100; N. variants: 14
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: rs34779708
rs34779708
0.827 0.120 10 35177257 intron variant T/G snv 0.33
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 2 2016 2017
dbSNP: rs34779708
rs34779708
0.827 0.120 10 35177257 intron variant T/G snv 0.33
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.700 1.000 2 2015 2017
dbSNP: rs34779708
rs34779708
0.827 0.120 10 35177257 intron variant T/G snv 0.33
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs34779708
rs34779708
0.827 0.120 10 35177257 intron variant T/G snv 0.33
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1.000 1 2016 2016
dbSNP: rs34779708
rs34779708
0.827 0.120 10 35177257 intron variant T/G snv 0.33
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs34779708
rs34779708
0.827 0.120 10 35177257 intron variant T/G snv 0.33
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1057108
rs1057108
1.000 0.080 10 35196021 5 prime UTR variant T/G snv 0.34 0.34
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1148247
rs1148247
0.882 0.160 10 35208018 intron variant G/A snv 0.33
CUI: C1847540
Disease: Azoospermia, Nonobstructive
Azoospermia, Nonobstructive
Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1148247
rs1148247
0.882 0.160 10 35208018 intron variant G/A snv 0.33
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1148247
rs1148247
0.882 0.160 10 35208018 intron variant G/A snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs11592925
rs11592925
1.000 0.080 10 35136622 intron variant C/T snv 0.14
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs12765063
rs12765063
10 35127641 intron variant G/A snv 0.14
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs12765063
rs12765063
10 35127641 intron variant G/A snv 0.14
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12775799
rs12775799
1.000 0.040 10 35199336 intron variant C/T snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs16935888
rs16935888
1.000 0.040 10 35143477 intron variant T/C snv 0.15
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs17583959
rs17583959
1.000 0.120 10 35133175 intron variant G/A snv 0.14
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2295415
rs2295415
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2295415
rs2295415
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19
CUI: C0024143
Disease: Lupus Nephritis
Lupus Nephritis
Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2295415
rs2295415
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19
CUI: C1847540
Disease: Azoospermia, Nonobstructive
Azoospermia, Nonobstructive
Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2384352
rs2384352
1.000 0.120 10 35203904 intron variant A/G snv 0.32
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4934540
rs4934540
1.000 0.040 10 35185771 intron variant T/C snv 0.33
CUI: C1847540
Disease: Azoospermia, Nonobstructive
Azoospermia, Nonobstructive
Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs4934735
rs4934735
1.000 0.040 10 35207802 intron variant A/G snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs58468612
rs58468612
10 35207699 intron variant G/A snv 0.14
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6481941
rs6481941
1.000 0.040 10 35151213 intron variant G/A snv 0.37
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2012 2012