CMIP, c-Maf inducing protein, 80790

N. diseases: 54; N. variants: 28
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: rs16955379
rs16955379 		1.000 0.080 16 81455768 intron variant C/T snv 3.6E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.810 1.000 2 2011 2019
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 9 2010 2019
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.800 1.000 2 2012 2014
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.710 1.000 4 2017 2018
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 3 2018 2019
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2018 2019
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs56823429
rs56823429 		16 81500184 intron variant C/A;G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2015 2018
dbSNP: rs11644696
rs11644696 		16 81538488 intron variant G/A;C;T snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs12596103
rs12596103 		1.000 0.080 16 81456948 intron variant C/T snv 1.4E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs12928482
rs12928482 		16 81480266 intron variant G/A snv 0.23
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12928482
rs12928482 		16 81480266 intron variant G/A snv 0.23
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs12930850
rs12930850 		16 81568607 intron variant A/G snv 0.38
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs149523885
rs149523885 		16 81559144 intron variant AGA/- delins 8.5E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs16955754
rs16955754 		1.000 0.040 16 81699303 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1820233
rs1820233 		1.000 0.040 16 81698903 intron variant A/G snv 1.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2012502
rs2012502 		16 81694476 intron variant C/A snv 0.39
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2317497
rs2317497 		16 81695004 intron variant A/T snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2911280
rs2911280 		1.000 0.080 16 81557708 intron variant A/G snv 0.82
CUI: C0201983
Disease: Dehydroepiandrosterone sulfate measurement (procedure)
Dehydroepiandrosterone sulfate measurement (procedure) 		0.700 1.000 1 2017 2017
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2925979
rs2925979 		1.000 0.080 16 81501185 intron variant T/A;C snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs34895689
rs34895689 		16 81688927 intron variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3751858
rs3751858 		1.000 0.040 16 81701272 intron variant T/G snv 8.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017