Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786204848
DDX58
0.882 0.040 9 32488884 missense variant C/A snv 4
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 4
rs1057518956
ZEB1
0.925 0.080 10 31520308 stop gained C/T snv 3
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 3
rs121909194
MYOC ; MYOCOS
0.882 0.040 1 171636302 missense variant C/G snv 3
rs17752199 0.925 0.040 6 51542050 upstream gene variant A/C;G;T snv 3
rs3766355
PTGFR
0.882 0.040 1 78491756 intron variant C/A;T snv 3
rs690037
RFTN1 ; OXNAD1
0.882 0.040 3 16354161 intron variant C/G;T snv 3
rs74315331
MYOC ; MYOCOS
0.882 0.040 1 171636010 missense variant A/C;T snv 3
rs74315332
MYOCOS ; MYOC
0.882 0.040 1 171636000 missense variant G/T snv 3
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 3
rs1057518844
CREBBP
1.000 0.040 16 3757288 missense variant C/T snv 2
rs121909193
MYOCOS ; MYOC
0.925 0.040 1 171636349 missense variant C/A snv 2
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 2
rs13178997
WDR36
0.925 0.040 5 111108550 intron variant G/A;T snv 2
rs1554200992
GJA1
0.925 0.160 6 121446966 missense variant C/T snv 2
rs200710076
OPTN
0.925 0.040 10 13109198 missense variant C/A;G;T snv 8.0E-06; 2.0E-05; 2.4E-05 2
rs2028386
LOXL1
1.000 0.040 15 73934367 intron variant C/A;G snv 2
rs28500712
AFAP1
1.000 0.040 4 7894486 intron variant A/C;G snv 2
rs28520091
AFAP1
1.000 0.040 4 7844513 intron variant C/A;G;T snv 2
rs28795989
AFAP1
1.000 0.040 4 7889818 intron variant A/C;G snv 2
rs4241366
SLCO2A1
0.925 0.040 3 134031326 intron variant G/A;C;T snv 2
rs74315337
MYOC
0.925 0.040 1 171652476 stop gained G/A;C;T snv 7.2E-04; 4.0E-06; 4.0E-06 2
rs9309969
CADM2
1.000 0.040 3 85085406 intron variant T/C;G snv 2
rs1013278 1.000 0.040 7 117963766 regulatory region variant G/A;C snv 1