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: rs12777
rs12777
SLC22A4 ; MIR3936HG
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 1 2009 2016
dbSNP: rs273909
rs273909
SLC22A4 ; MIR3936HG
1.000 0.040 5 132331660 intron variant A/G snv 9.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.800 1.000 1 2013 2018
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 132341949 intron variant A/G snv 0.31
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 132341949 intron variant A/G snv 0.31
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 132341949 intron variant A/G snv 0.31
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 132341949 intron variant A/G snv 0.31
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs10075801
rs10075801
SLC22A4 ; MIR3936HG
5 132341949 intron variant A/G snv 0.31
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs10479002
rs10479002
SLC22A4 ; MIR3936HG
5 132335969 synonymous variant C/G snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2009 2009
dbSNP: rs1050152
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28
CUI: C0027430
Disease: Nasal Polyps
Nasal Polyps 		0.700 1.000 1 2019 2019
dbSNP: rs11950562
rs11950562
SLC22A4 ; MIR3936HG
5 132316836 intron variant A/C snv 0.37
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs12777
rs12777
SLC22A4 ; MIR3936HG
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
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: rs270601
rs270601
SLC22A4 ; MIR3936HG
5 132321304 intron variant T/C snv 0.71
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		0.700 1.000 1 2015 2015
dbSNP: rs270602
rs270602
SLC22A4 ; MIR3936HG
5 132321007 intron variant T/A;C snv
CUI: C0523446
Disease: Acylcarnitines measurement
Acylcarnitines measurement 		0.700 1.000 1 2015 2015
dbSNP: rs272869
rs272869
SLC22A4 ; MIR3936HG
5 132342304 intron variant A/G snv 0.64
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs272869
rs272869
SLC22A4 ; MIR3936HG
5 132342304 intron variant A/G snv 0.64
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs34301845
rs34301845
SLC22A4 ; MIR3936HG
5 132329474 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTTTT delins 0.56
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs34301845
rs34301845
SLC22A4 ; MIR3936HG
5 132329474 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTTTT delins 0.56
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs419291
rs419291
SLC22A4
5 132297662 intron variant T/A;C snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs538021413
rs538021413
SLC22A4 ; MIR3936HG
5 132328824 intron variant TATATATATATA/-;TA;TATA;TATATA;TATATATA;TATATATATA;TATATATATATATA;TATATATATATATATA delins 0.39
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs56399423
rs56399423
SLC22A4 ; MIR3936HG
5 132336964 intron variant T/C snv 0.28
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs6860806
rs6860806
SLC22A4
1.000 0.080 5 132304843 intron variant A/C;G snv 0.46
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017