Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1476679
ZCWPW1
0.925 0.080 7 100406823 intron variant C/A;T snv 4.0E-06; 0.74 2
rs1050286
OLR1
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3
rs17808009
OLR1
1.000 0.080 12 10159330 3 prime UTR variant C/T snv 0.42 1
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4
rs139709573
TM2D3
1.000 0.080 15 101646763 missense variant G/A snv 2.9E-04 1.4E-04 1
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs4669573
HPCAL1
1.000 0.080 2 10338810 intron variant A/G snv 0.47 1
rs10197851
HPCAL1
1.000 0.080 2 10345283 intron variant A/G snv 0.52 1
rs760832624
CALHM1
0.882 0.120 10 103458488 frameshift variant CAGCGGCC/- delins 3
rs2986017
CALHM1
0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs386747134
CALHM1
0.882 0.120 10 103458495 missense variant AGC/GGT mnv 3
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs770510230
ABCA7
1.000 0.080 19 1058155 stop gained G/T snv 2.0E-05 4.2E-05 1
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs17277986
SORCS1
0.925 0.080 10 106998968 intron variant C/T snv 0.22 2
rs950809
SORCS1
1.000 0.080 10 107035617 intron variant A/G snv 0.48 1
rs80001089
UNG
1.000 0.080 12 109099757 intron variant T/G snv 5.8E-02 1
rs2569987
UNG
1.000 0.080 12 109103366 intron variant T/C snv 0.12 1
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1035071612
MIR6886 ; LDLR
0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs760678
LOC105374925 ; NEDD9
0.882 0.080 6 11334421 intron variant C/G;T snv 3
rs1799999
PPP1R3A
0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17 4