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: rs17643262
rs17643262
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 3 2011 2018
dbSNP: rs346763
rs346763
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 2 2014 2018
dbSNP: rs17356664
rs17356664
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: rs10416371
rs10416371
1.000 0.080 19 45156878 intron variant A/C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 2 2011 2012
dbSNP: rs12461144
rs12461144
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
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
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
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
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
0.925 0.040 19 45121045 intron variant A/G snv 0.15
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs10415983
rs10415983
1.000 0.080 19 45208340 intron variant C/T snv 0.26
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs10421247
rs10421247
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: rs10422797
rs10422797
1.000 0.080 19 45222848 intron variant T/C snv 8.9E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs1048699
rs1048699
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs1048699
rs1048699
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs11083766
rs11083766
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
19 45212232 intron variant T/C snv 0.26
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016
dbSNP: rs111243475
rs111243475
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: rs1114831
rs1114831
1.000 0.080 19 45133061 intron variant C/A snv 9.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs1114832
rs1114832
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs1114832
rs1114832
1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs11667509
rs11667509
19 45212934 3 prime UTR variant G/C snv 0.28
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs11667829
rs11667829
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
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: rs11669910
rs11669910
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