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: rs8100183
rs8100183
1.000 0.080 19 45081434 intron variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs78620885
rs78620885
1.000 0.080 19 45087826 intron variant C/T snv 3.1E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs9653111
rs9653111
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: rs138137383
rs138137383
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: rs12461065
rs12461065
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: 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: 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: rs145903417
rs145903417
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
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 1 2011 2018
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: rs536518226
rs536518226
1.000 0.080 19 45137507 intron variant G/C snv 7.8E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs28469095
rs28469095
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: 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: rs149553138
rs149553138
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
dbSNP: rs12463049
rs12463049
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: 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: rs2159324
rs2159324
19 45192480 intron variant T/C snv 0.36
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2009 2009
dbSNP: rs149495476
rs149495476
1.000 0.080 19 45193381 intron variant G/T snv 1.2E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs620807
rs620807
1.000 0.080 19 45203694 intron variant A/G snv 0.47
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
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: rs73566293
rs73566293
1.000 0.080 19 45209421 intron variant G/A snv 4.0E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
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: rs3803906
rs3803906
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: 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