Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs2069718
IFNG ; IFNG-AS1
0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs2735971
MRPL23 ; H19
0.790 0.240 11 2000419 intron variant T/C snv 7
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 6
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs7660895
SLC2A9
0.882 0.200 4 9983821 intron variant A/G;T snv 5
rs10733376
CDKN2B-AS1
1.000 0.080 9 22114470 intron variant G/C snv 0.64 3
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 3
rs595244
FBN1
0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs727333
DSCAM
1.000 0.080 21 40331020 intron variant C/A snv 6.6E-02 3
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs11777927
TOX
1.000 0.080 8 58968480 intron variant A/C;T snv 2
rs3783107
COL4A1
1.000 0.080 13 110189755 intron variant G/A snv 0.36 2
rs700651
BOLL
1.000 0.080 2 197766990 intron variant G/A snv 0.73 2
rs10230207 1.000 0.080 7 19571684 intron variant G/C;T snv 1
rs111610752
HLCS
1.000 0.080 21 36778953 intron variant A/C;T snv 1.8E-02 1