Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10746463
CD55
0.851 0.200 1 207337251 missense variant G/A;T snv 4
rs10787498
CASP7
0.925 0.080 10 113729891 3 prime UTR variant T/G snv 0.38 2
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs11040869 0.925 0.080 11 1263382 downstream gene variant G/A snv 1.8E-02 2
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs1108143 1.000 0.080 2 234557214 regulatory region variant A/G snv 8.1E-02 1
rs11084490
AURKC
0.925 0.080 19 57231104 5 prime UTR variant G/A;C;T snv 0.87; 3.8E-05 2
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs111238176
FASLG
0.851 0.160 1 172665840 missense variant A/G snv 4
rs11133399
CLOCK
0.925 0.080 4 55547664 non coding transcript exon variant A/G snv 0.28 2
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs111638916
PSMD10
0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs11170877
COPZ1
0.925 0.080 12 54340505 start lost A/G snv 0.16 0.17 2
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs112310158
MIR449B ; MIR449A ; CDC20B
0.925 0.080 5 55170550 non coding transcript exon variant G/A snv 1.7E-03 7.5E-03 2
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs11254413
TRDMT1
0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44 4
rs1126757
IL11
0.882 0.120 19 55368504 synonymous variant C/G;T snv 4.1E-06; 0.48 3
rs1126760
FAM71E2 ; IL11
0.925 0.080 19 55364706 3 prime UTR variant G/A;C snv 2
rs1126772
SPP1
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16 5
rs1127379
SFRP1
0.882 0.120 8 41263761 3 prime UTR variant T/C snv 0.48 3
rs112754928
SPOCD1
0.925 0.080 1 31815123 missense variant G/A;T snv 4.5E-03; 1.2E-05 2