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: rs12604324
rs12604324
1 1.000 0.080 18 24164468 intron variant G/A snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs1741309
rs1741309
1 1.000 0.080 20 4163930 intron variant A/G snv 0.53 0.700 1.000 1 2014 2014
dbSNP: rs41526548
rs41526548
1 1.000 0.080 9 92129496 upstream gene variant T/C snv 0.700 1.000 1 2014 2014
dbSNP: rs112451138
rs112451138
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
2 0.925 0.080 6 151966232 intron variant T/C snv 0.75 0.010 1.000 1 2014 2014
dbSNP: rs2337506
rs2337506
2 0.925 0.080 15 32053864 intron variant A/G snv 0.60 0.010 1.000 1 2017 2017
dbSNP: rs3087258
rs3087258
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: rs3824968
rs3824968
2 0.925 0.080 11 121605213 synonymous variant T/A snv 0.39 0.29 0.010 1.000 1 2009 2009
dbSNP: rs63750324
rs63750324
2 0.925 0.080 14 73198111 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs8027814
rs8027814
2 0.925 0.080 15 32058469 intron variant G/A snv 0.57 0.010 1.000 1 2017 2017
dbSNP: rs1010159
rs1010159
3 0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 0.010 1.000 1 2009 2009
dbSNP: rs1043202
rs1043202
3 0.882 0.080 12 54182178 missense variant T/A snv 0.010 1.000 1 2008 2008
dbSNP: rs1341026713
rs1341026713
APP
3 0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs142690225
rs142690225
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
3 0.882 0.120 20 1989288 intron variant A/G snv 0.40 0.010 1.000 1 2009 2009
dbSNP: rs2420616
rs2420616
3 0.882 0.080 10 119316984 intron variant A/G snv 0.69 0.010 1.000 1 2015 2015
dbSNP: rs2618516
rs2618516
3 0.882 0.080 11 14000092 intron variant T/C snv 0.65 0.010 1.000 1 2013 2013
dbSNP: rs4752293
rs4752293
3 0.882 0.080 10 119342186 intron variant C/T snv 0.74 0.010 1.000 1 2015 2015
dbSNP: rs4879809
rs4879809
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
3 0.882 0.120 14 73171047 missense variant T/A;C snv 0.010 1.000 1 2000 2000