Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5744105 0.925 0.080 1 223142735 intron variant G/C snv 0.57 2
rs5743867 0.882 0.120 11 1307121 intron variant G/A;C snv 3
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs5743551 0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs506027 0.925 0.080 6 106326589 upstream gene variant G/A snv 0.57 2
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs497116 0.925 0.080 11 104892390 stop lost A/G snv 4.3E-02 2
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4755453 0.925 0.080 11 36509094 intron variant C/A;G;T snv 2
rs4684846 0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs414171 0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs41279766 0.925 0.080 2 118970217 missense variant C/G;T snv 2.1E-03 2
rs41274221 0.851 0.160 7 100093577 mature miRNA variant C/T snv 6.4E-05 4.9E-05 6
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs374520012
LBP
0.882 0.120 20 38373994 missense variant T/C;G snv 8.0E-06; 4.0E-06 3
rs368287711 0.851 0.120 11 117989554 missense variant C/A;T snv 2.0E-05; 2.4E-05 4