Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs145204276
ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76
0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs11801299
LOC105371692
0.807 0.200 1 204559956 downstream gene variant G/A snv 0.16 9
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs1332018
GSTM5 ; GSTM3
0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs201701502
DDR2
0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 5
rs1172398253
CCN1
0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs3917412
C1orf112 ; SELE
1.000 0.040 1 169731361 intron variant T/A;C;G snv 4
rs1196644309
TXNIP
1.000 0.080 1 145995155 missense variant G/A snv 3
rs772092699
EPHB2
0.925 0.080 1 22912497 missense variant C/A;G;T snv 4.0E-06 3
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs1223118092
LOC100506142 ; RHOQ
2 46576601 missense variant A/G snv 1
rs6737848
SOCS5 ; LINC01118
2 46701027 intron variant C/G snv 0.14 1