Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7815950
SNX31
1.000 0.040 8 100646940 intron variant A/G snv 6.6E-02 1
rs1336698
FGF14
1.000 0.040 13 102211398 intron variant C/T snv 0.85 1
rs748910652
NFKB2
1.000 0.040 10 102400759 stop gained C/T snv 8.2E-06 1
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs9690688
LOC105375446 ; LAMB4
1.000 0.040 7 108079717 missense variant C/A snv 8.9E-02 0.17 1
rs375099
RANBP2
1.000 0.040 2 109043821 intergenic variant G/A;C snv 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs17140937 1.000 0.040 7 118148430 intergenic variant T/C snv 6.0E-02 1
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs5977837 1.000 0.040 X 133235903 downstream gene variant T/C snv 0.11 1
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs2682665 1.000 0.040 8 13940496 intergenic variant C/A;T snv 1
rs6649722 1.000 0.040 X 144310656 upstream gene variant C/T snv 4.0E-02 1
rs5987017
ATP2B3
1.000 0.040 X 153516714 upstream gene variant A/G snv 1
rs10038271
HAVCR1
1.000 0.040 5 157043390 intron variant C/T snv 0.16 1
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14