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: rs56823429
rs56823429
16 81500184 intron variant C/A;G;T snv
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: 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: 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: 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: rs4889341
rs4889341
16 81570646 intron variant T/C snv 0.52
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs56320921
rs56320921
16 81479155 intron variant C/T snv 4.8E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs56823429
rs56823429
16 81500184 intron variant C/A;G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs57159061
rs57159061
16 81557357 intron variant T/C snv 0.11
Dehydroepiandrosterone sulfate measurement (procedure)
0.700 1.000 1 2019 2019
dbSNP: rs62046625
rs62046625
16 81545101 intron variant G/A snv 0.12
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs8059962
rs8059962
16 81540592 intron variant T/C snv 0.52
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs2925979
rs2925979
1.000 0.080 16 81501185 intron variant T/A;C snv
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
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: rs16955379
rs16955379
1.000 0.080 16 81455768 intron variant C/T snv 3.6E-02
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: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
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: rs12596103
rs12596103
1.000 0.080 16 81456948 intron variant C/T snv 1.4E-02
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2011 2011
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