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: 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: rs12461144
rs12461144
MARK4 ; EXOC3L2
1.000 0.080 19 45220448 intron variant C/T snv 0.22
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 2 2018 2019
dbSNP: rs595290
rs595290
MARK4 ; BLOC1S3
1.000 0.080 19 45205150 intron variant T/C snv 0.27
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 2 2018 2019
dbSNP: rs62118504
rs62118504
MARK4 ; EXOC3L2
1.000 0.080 19 45231493 intron variant A/G snv 0.32
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 2 2018 2019
dbSNP: rs10408847
rs10408847
MARK4 ; PPP1R37
1.000 0.080 19 45131424 intron variant G/C snv 0.26
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs10409138
rs10409138
MARK4 ; PPP1R37
0.925 0.040 19 45121045 intron variant A/G snv 0.15
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs10409138
rs10409138
MARK4 ; PPP1R37
0.925 0.040 19 45121045 intron variant A/G snv 0.15
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs10421247
rs10421247
MARK4 ; NKPD1 ; LOC105372420
1.000 0.080 19 45154228 intron variant C/T snv 0.52
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
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: rs111243475
rs111243475
MARK4 ; BLOC1S3
1.000 0.080 19 45188312 intron variant C/T snv 4.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
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: rs11667829
rs11667829
MARK4 ; EXOC3L2
1.000 0.080 19 45236417 intron variant G/A snv 0.25
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
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: rs11669915
rs11669915
MARK4 ; EXOC3L2
19 45238095 intron variant A/G snv 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs11673000
rs11673000
MARK4 ; EXOC3L2
19 45238753 missense variant C/G;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs11673000
rs11673000
MARK4 ; EXOC3L2
19 45238753 missense variant C/G;T snv
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: rs11673093
rs11673093
MARK4 ; EXOC3L2
1.000 0.040 19 45238836 synonymous variant G/A snv 0.22
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs11673093
rs11673093
MARK4 ; EXOC3L2
1.000 0.040 19 45238836 synonymous variant G/A snv 0.22
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
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