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: rs112451138
rs112451138
PSEN1
2 0.925 0.080 14 73192667 missense variant T/C snv 7.0E-06 0.010 1.000 1 2015 2015
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: 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: rs3087258
rs3087258
IL1B
2 0.925 0.080 2 112837294 upstream gene variant G/A snv 0.010 1.000 1 2012 2012
dbSNP: rs373885474
rs373885474
GRN
2 0.925 0.080 17 44352061 missense variant C/A;T snv 7.2E-05 0.010 1.000 1 2013 2013
dbSNP: rs63750324
rs63750324
PSEN1
2 0.925 0.080 14 73198111 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs8027814
rs8027814
CHRNA7
2 0.925 0.080 15 32058469 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017
dbSNP: rs1043202
rs1043202
SMUG1
3 0.882 0.080 12 54182178 missense variant T/A snv 0.010 1.000 1 2008 2008
dbSNP: rs142690225
rs142690225
PSEN2
3 0.925 0.080 1 226894111 missense variant G/A snv 1.1E-04 1.1E-04 0.010 1.000 1 2008 2008
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: 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: 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: rs4752293
rs4752293
GRK5
3 0.882 0.080 10 119342186 intron variant C/T snv 0.74 0.010 1.000 1 2015 2015
dbSNP: rs4879809
rs4879809
SIGMAR1
3 0.882 0.120 9 34635601 3 prime UTR variant T/A;C;G snv 1.1E-03; 1.00 0.010 1.000 1 2015 2015
dbSNP: rs529782627
rs529782627
APP
3 0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs533667466
rs533667466
APP
3 0.925 0.080 21 25911912 missense variant T/C snv 0.010 1.000 1 2008 2008
dbSNP: rs553119528
rs553119528
GRN
3 0.882 0.160 17 44352489 missense variant G/A snv 5.2E-05 6.3E-05 0.010 1.000 1 2010 2010
dbSNP: rs63750151
rs63750151
APP
3 0.882 0.080 21 25891761 missense variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs63751399
rs63751399
PSEN1
3 0.882 0.120 14 73171047 missense variant T/A;C snv 0.010 1.000 1 2000 2000
dbSNP: rs6489630
rs6489630
NTF3
3 0.882 0.080 12 5495458 intron variant T/C snv 0.75 0.010 1.000 1 2012 2012
dbSNP: rs748703149
rs748703149
APOE
3 0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 0.010 < 0.001 1 2020 2020
dbSNP: rs766647311
rs766647311
TREM2 ; TREML1 ; LOC105375056
3 0.882 0.080 6 41159841 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 < 0.001 1 2020 2020
dbSNP: rs767425642
rs767425642
ACE
3 0.882 0.120 17 63489010 missense variant G/A;T snv 3.2E-05; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs8126696
rs8126696 		3 0.882 0.080 21 37358422 intron variant T/C snv 0.64 0.010 1.000 1 2012 2012
dbSNP: rs901115236
rs901115236
CHCHD10 ; LOC107985577
3 0.882 0.120 22 23767531 missense variant G/A;T snv 1.5E-05; 1.5E-05 0.010 1.000 1 2017 2017