Source: CURATED

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: 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: 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: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		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: 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: rs12971645
rs12971645
MARK4
19 45304687 3 prime UTR variant G/A snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs28469095
rs28469095
MARK4 ; NKPD1 ; LOC105372420
1.000 0.080 19 45152075 missense variant T/C snv 0.11 9.1E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs346757
rs346757
MARK4 ; EXOC3L2
1.000 0.080 19 45222190 intron variant G/C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
dbSNP: rs3803906
rs3803906
MARK4 ; EXOC3L2 ; BLOC1S3
19 45212718 3 prime UTR variant A/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs62118504
rs62118504
MARK4 ; EXOC3L2
1.000 0.080 19 45231493 intron variant A/G snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs73036519
rs73036519
MARK4 ; EXOC3L2
0.851 0.040 19 45245104 intron variant G/A;C snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs9653111
rs9653111
MARK4 ; GEMIN7 ; GEMIN7-AS1
1.000 0.080 19 45089217 intron variant C/T snv 9.9E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2019 2019
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: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		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: 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: 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: 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: rs12461065
rs12461065
MARK4 ; PPP1R37
1.000 0.080 19 45102050 intron variant C/T snv 0.50
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs12463049
rs12463049
MARK4 ; BLOC1S3
1.000 0.080 19 45187692 non coding transcript exon variant C/G snv 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs138137383
rs138137383
MARK4 ; PPP1R37
1.000 0.080 19 45098343 intron variant G/A;C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs145903417
rs145903417
MARK4 ; PPP1R37
1.000 0.080 19 45125846 intron variant A/G snv 1.3E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018