Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs76112240
rs76112240
MECOM
3 169418126 intron variant A/C snv 0.12
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs6770911
rs6770911
MECOM
3 169577976 intron variant A/C;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs6770911
rs6770911
MECOM
3 169577976 intron variant A/C;G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs73174306
rs73174306
MECOM ; MECOM-AS1
3 169476456 intron variant A/C;G;T snv 2.8E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs998749
rs998749
MECOM
3 169255014 intron variant A/G snv 0.40
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs12632583
rs12632583
MECOM ; MECOM-AS1
1.000 0.040 3 169464399 intron variant A/G snv 4.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12634933
rs12634933
MECOM
3 169312191 intron variant A/G snv 8.1E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2015 2015
dbSNP: rs142436749
rs142436749
MECOM
1.000 0.080 3 169375312 intron variant A/G snv 7.7E-03
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs1918973
rs1918973
MECOM ; MECOM-AS1
3 169447385 intron variant A/G snv 0.57
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1918973
rs1918973
MECOM ; MECOM-AS1
3 169447385 intron variant A/G snv 0.57
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs76273615
rs76273615
MECOM
3 169374250 intron variant A/G snv 0.11
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2018 2018
dbSNP: rs78101726
rs78101726
MECOM
3 169577648 intron variant A/G snv 0.16
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs78101726
rs78101726
MECOM
3 169577648 intron variant A/G snv 0.16
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs78307470
rs78307470
MECOM
3 169139845 intron variant A/G snv 6.2E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs9290366
rs9290366
MECOM
3 169399217 intron variant A/G snv 0.57
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs9290366
rs9290366
MECOM
3 169399217 intron variant A/G snv 0.57
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs9290366
rs9290366
MECOM
3 169399217 intron variant A/G snv 0.57
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs1290790
rs1290790
MECOM
3 169373781 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1290790
rs1290790
MECOM
3 169373781 intron variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs784288
rs784288
MECOM
1.000 0.080 3 169253443 intron variant A/G;T snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.800 1.000 1 2013 2013
dbSNP: rs4955659
rs4955659
MECOM ; MECOM-AS1
1.000 0.040 3 169453830 intron variant A/T snv 4.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10711289
rs10711289
MECOM ; MECOM-AS1
3 169450583 intron variant AAA/-;A;AA;AAAA;AAAAA delins
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1344555
rs1344555
MECOM
3 169582431 intron variant C/A;G;T snv
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2011 2011
dbSNP: rs1344555
rs1344555
MECOM
3 169582431 intron variant C/A;G;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2011 2011
dbSNP: rs11718956
rs11718956
MECOM
3 169640170 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019