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: rs5762813
rs5762813
22 28807326 intron variant C/T snv 0.25
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs5762862
rs5762862
22 28856744 intergenic variant G/A;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs5762862
rs5762862
22 28856744 intergenic variant G/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs5762862
rs5762862
22 28856744 intergenic variant G/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs62235753
rs62235753
1.000 0.080 22 28876649 intergenic variant C/T snv 1.3E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs62236881
rs62236881
22 29054205 3 prime UTR variant G/A snv 1.9E-03
CUI: C4048548
Disease: Anti-Mullerian Hormone Measurement
Anti-Mullerian Hormone Measurement
0.700 1.000 1 2019 2019
dbSNP: rs8141529
rs8141529
22 28873704 intergenic variant A/G snv 0.33
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs8142788
rs8142788
22 29004527 intron variant G/A snv 0.11
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs12321
rs12321
1.000 0.040 22 29057205 3 prime UTR variant G/C snv 0.38
CUI: C0271183
Disease: Severe myopia
Severe myopia
Eye Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs2269577
rs2269577
0.882 0.120 22 28800769 non coding transcript exon variant G/C snv 0.40
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2269577
rs2269577
0.882 0.120 22 28800769 non coding transcript exon variant G/C snv 0.40
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
Skin and Connective Tissue Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2269577
rs2269577
0.882 0.120 22 28800769 non coding transcript exon variant G/C snv 0.40
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2269577
rs2269577
0.882 0.120 22 28800769 non coding transcript exon variant G/C snv 0.40
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs7290117
rs7290117
0.925 0.040 22 29054868 3 prime UTR variant C/G;T snv
CUI: C0017605
Disease: Angle Closure Glaucoma
Angle Closure Glaucoma
Eye Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs7290117
rs7290117
0.925 0.040 22 29054868 3 prime UTR variant C/G;T snv
CUI: C0017606
Disease: Primary angle-closure glaucoma
Primary angle-closure glaucoma
Eye Diseases 0.010 < 0.001 1 2018 2018