Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs985421
SORL1
0.925 0.080 11 121491607 intron variant G/A snv 3.0E-02 2
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs9527025
KL
1.000 0.040 13 33054056 missense variant G/C;T snv 0.14 1
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs9340803
ESR1
0.925 0.080 6 151842832 intron variant A/G snv 1.0E-03 3.8E-04 2
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 5
rs8702
KLC1
0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs8063
UBE2I
1.000 0.040 16 1324817 3 prime UTR variant A/C;G snv 4.0E-06; 4.0E-06; 0.71 1
rs8052688
UBE2I
1.000 0.040 16 1322182 intron variant G/A;C snv 1
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 4
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs774321998
C1orf167 ; MTHFR
1.000 0.040 1 11790683 missense variant T/C snv 4.0E-06 7.0E-06 1
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs754203
CYP46A1
0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
rs7483
GSTM3 ; GSTM5
0.742 0.320 1 109737079 missense variant C/T snv 4.0E-06; 0.35 0.26 11
rs7354779
DNMT3L ; DNMT3L-AS1
0.827 0.200 21 44250887 missense variant T/C snv 0.21 6
rs702723
PLK2
0.925 0.080 5 58457629 non coding transcript exon variant C/T snv 0.67 0.66 2
rs6850306
LCORL
0.925 0.080 4 18004466 intron variant G/A snv 0.12 2
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs6598008
CDHR5
0.925 0.080 11 618172 intron variant A/G snv 0.48 2
rs641120
SORL1
0.882 0.080 11 121510256 intron variant G/A snv 0.38 3
rs640476 1.000 0.040 5 161277998 intergenic variant T/G snv 0.42 1
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23