Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800764
rs1800764 		10 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1884049
rs1884049
ESR1
2 0.925 0.080 6 151966232 intron variant T/C snv 0.75 0.010 1.000 1 2014 2014
dbSNP: rs193922916
rs193922916
APP
6 0.827 0.080 21 25897619 missense variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs1997794
rs1997794
PDYN ; PDYN-AS1
4 0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50 0.010 1.000 1 2009 2009
dbSNP: rs2200733
rs2200733 		12 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs223330
rs223330
CISD2
4 0.851 0.160 4 102872502 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs223331
rs223331
CISD2
5 0.851 0.160 4 102872408 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs2235751
rs2235751
PDYN ; PDYN-AS1
3 0.882 0.120 20 1989288 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
dbSNP: rs2276109
rs2276109
MMP12
18 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.010 < 0.001 1 2018 2018
dbSNP: rs2306604
rs2306604
TFAM
5 0.827 0.080 10 58388932 intron variant A/C;G;T snv 0.010 < 0.001 1 2013 2013
dbSNP: rs2337506
rs2337506
CHRNA7
2 0.925 0.080 15 32053864 intron variant A/G snv 0.60 0.010 1.000 1 2017 2017
dbSNP: rs2420616
rs2420616
GRK5
3 0.882 0.080 10 119316984 intron variant A/G snv 0.69 0.010 1.000 1 2015 2015
dbSNP: rs242557
rs242557
MAPT
12 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2019 2019
dbSNP: rs2618516
rs2618516
SPON1
3 0.882 0.080 11 14000092 intron variant T/C snv 0.65 0.010 1.000 1 2013 2013
dbSNP: rs267606673
rs267606673
ATP7A ; PGK1
9 0.776 0.240 X 78029314 missense variant C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs2695121
rs2695121
NR1H2
16 0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 0.010 1.000 1 2017 2017
dbSNP: rs3087258
rs3087258
IL1B
2 0.925 0.080 2 112837294 upstream gene variant G/A snv 0.010 1.000 1 2012 2012
dbSNP: rs3093059
rs3093059
CRP
11 0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs334558
rs334558
GSK3B ; LOC107986119
20 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs3764435
rs3764435
ALDH1A1
5 0.827 0.120 9 72901960 intron variant A/C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs3764650
rs3764650
ABCA7
9 0.790 0.200 19 1046521 intron variant T/G snv 0.14 0.010 1.000 1 2019 2019
dbSNP: rs387906709
rs387906709
UBQLN2
9 0.776 0.120 X 56565363 missense variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2004 2004
dbSNP: rs405509
rs405509
APOE
30 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 0.010 < 0.001 1 2019 2019
dbSNP: rs4291
rs4291
ACE
20 0.724 0.400 17 63476833 upstream gene variant T/A;C snv 0.010 1.000 1 2017 2017