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: rs2159324
rs2159324
MARK4 ; BLOC1S3
19 45192480 intron variant T/C snv 0.36
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2009 2009
dbSNP: rs17356664
rs17356664
MARK4 ; EXOC3L2
19 45237513 intron variant C/T snv 0.28
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs17643262
rs17643262
MARK4 ; PPP1R37
1.000 0.080 19 45128558 intron variant G/A snv 9.9E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2011 2018
dbSNP: rs346763
rs346763
MARK4 ; EXOC3L2
1.000 0.080 19 45226017 intron variant G/A snv 0.10
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2014 2018
dbSNP: rs11083766
rs11083766
MARK4 ; EXOC3L2 ; BLOC1S3
19 45212232 intron variant T/C snv 0.26
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11083766
rs11083766
MARK4 ; EXOC3L2 ; BLOC1S3
19 45212232 intron variant T/C snv 0.26
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11667509
rs11667509
MARK4 ; EXOC3L2 ; BLOC1S3
19 45212934 3 prime UTR variant G/C snv 0.28
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs11669910
rs11669910
MARK4 ; EXOC3L2
19 45238075 intron variant A/T snv 0.23
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs11669910
rs11669910
MARK4 ; EXOC3L2
19 45238075 intron variant A/T snv 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12459847
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs12459847
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs12459847
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12982781
rs12982781
MARK4
19 45283297 intron variant T/C snv 0.33
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs145605569
rs145605569
MARK4 ; EXOC3L2
19 45239644 intron variant C/T snv 0.21
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs151165225
rs151165225
MARK4
19 45257662 intron variant C/T snv 0.19
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7255933
rs7255933
MARK4
19 45263471 intron variant G/A snv 0.19
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs73036517
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs73036517
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs73036517
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs73036517
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs73036519
rs73036519
MARK4 ; EXOC3L2
0.851 0.040 19 45245104 intron variant G/A;C snv
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs73036519
rs73036519
MARK4 ; EXOC3L2
0.851 0.040 19 45245104 intron variant G/A;C snv
CUI: C0271084
Disease: Exudative age-related macular degeneration
Exudative age-related macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs73036519
rs73036519
MARK4 ; EXOC3L2
0.851 0.040 19 45245104 intron variant G/A;C snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.700 1.000 1 2016 2016
dbSNP: rs73036519
rs73036519
MARK4 ; EXOC3L2
0.851 0.040 19 45245104 intron variant G/A;C snv
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy 		0.700 1.000 1 2016 2016
dbSNP: rs149553138
rs149553138
MARK4 ; TRAPPC6A
19 45169220 intron variant G/A snv 2.1E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2017 2017