Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs3741378
SIPA1
0.851 0.080 11 65641466 missense variant C/G;T snv 0.15 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 7
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2071410
FURIN
0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs7753826 0.925 0.120 6 26042011 upstream gene variant T/A;C snv 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6