ZNRF3, zinc and ring finger 3, 84133

N. diseases: 41; N. variants: 21
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: rs4823006
rs4823006
22 29055683 3 prime UTR variant A/G snv 0.41
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.800 1.000 2 2010 2019
dbSNP: rs2294239
rs2294239
22 29053489 intron variant A/G snv 0.36
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 3 2018 2019
dbSNP: rs12321
rs12321
1.000 0.040 22 29057205 3 prime UTR variant G/C snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 2 2019 2019
dbSNP: rs16986825
rs16986825
1.000 0.120 22 28904318 intron variant C/T snv 0.13
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 2 2014 2018
dbSNP: rs5762862
rs5762862
22 28856744 intergenic variant G/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 2 2018 2018
dbSNP: rs115770674
rs115770674
22 28860678 intergenic variant G/A snv 6.3E-02
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs13054095
rs13054095
1.000 0.080 22 29010231 intron variant A/T snv 1.6E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs13056243
rs13056243
22 28953318 intron variant C/T snv 0.13
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs143012756
rs143012756
22 28914537 intron variant G/A snv 3.2E-03
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs143012756
rs143012756
22 28914537 intron variant G/A snv 3.2E-03
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs16986861
rs16986861
22 28947200 intron variant G/A;C snv 0.13
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs16986864
rs16986864
22 28954923 intron variant G/T snv 0.13
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs2179129
rs2179129
22 29054935 3 prime UTR variant A/G snv 0.34
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2015 2015
dbSNP: rs2179129
rs2179129
22 29054935 3 prime UTR variant A/G snv 0.34
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs2294239
rs2294239
22 29053489 intron variant A/G snv 0.36
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2294239
rs2294239
22 29053489 intron variant A/G snv 0.36
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs2294239
rs2294239
22 29053489 intron variant A/G snv 0.36
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs34923414
rs34923414
22 28820734 intron variant C/T snv 0.67
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs4055
rs4055
22 28956507 intron variant A/C snv 0.13
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs4823006
rs4823006
22 29055683 3 prime UTR variant A/G snv 0.41
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs4823006
rs4823006
22 29055683 3 prime UTR variant A/G snv 0.41
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs4823006
rs4823006
22 29055683 3 prime UTR variant A/G snv 0.41
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs4823006
rs4823006
22 29055683 3 prime UTR variant A/G snv 0.41
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs5762813
rs5762813
22 28807326 intron variant C/T snv 0.25
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs5762813
rs5762813
22 28807326 intron variant C/T snv 0.25
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019