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: rs10058074
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2013 2013
dbSNP: rs10058074
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
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: rs147858478
rs147858478
MIR3936HG
5 132347093 intron variant GAGTTCT/-;GAGTTCTGAGTTCT delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs2631367
rs2631367
SLC22A5 ; MIR3936HG
0.925 0.120 5 132369766 5 prime UTR variant C/G snv 0.59
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		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: rs274546
rs274546
MIR3936HG
5 132364175 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
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: rs4705938
rs4705938
MIR3936HG
5 132358384 intron variant T/C snv 0.34
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019