Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs10208770
SP110
1.000 0.080 2 230170151 intron variant T/G snv 0.14 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10498244
SP110
1.000 0.080 2 230173117 non coding transcript exon variant T/C snv 0.26 1
rs10499859
CD36
0.925 0.120 7 80629494 intron variant A/G snv 0.46 2
rs1050504
NSMAF
1.000 0.080 8 58583857 3 prime UTR variant C/T snv 0.24 1
rs1057141
PSMB9 ; TAP1
1.000 0.080 6 32850997 missense variant T/C snv 0.20 0.20 1
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs10841845
CLEC4E
0.925 0.200 12 8533837 3 prime UTR variant A/G snv 0.28 2
rs10841847
CLEC4E
1.000 0.080 12 8535216 intron variant A/G snv 0.58 1
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11003125
MBL2
0.790 0.480 10 52772254 upstream gene variant G/C snv 0.31 7
rs11168287
VDR
0.882 0.160 12 47891631 intron variant G/A snv 0.56 3
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1135216
PSMB9 ; TAP1
0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 6
rs1135791
SP110
0.925 0.080 2 230177560 missense variant A/G snv 0.42 0.40 2
rs1136452
SFTPA1
0.925 0.120 10 79612410 missense variant C/A;G;T snv 4.0E-06; 7.0E-03; 4.0E-06 2
rs11568350
SLC40A1
0.790 0.240 2 189565370 missense variant C/A snv 3.8E-03 1.6E-02 9
rs11574079
VDR
1.000 0.080 12 47858947 intron variant C/T snv 1.7E-03 1
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5