Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs10927875
ZBTB17
1.000 0.040 1 15972817 intron variant C/T snv 0.29 3
rs2043055
IL18
0.925 0.080 11 112160901 intron variant A/G;T snv 3
rs4746172
VCL
10 74096084 intron variant C/T snv 0.73 3
rs4149018
SLCO1B1
1.000 0.080 12 21138627 intron variant T/G snv 4.3E-02 2
rs12582717
SLCO1B1
12 21143872 intron variant C/G snv 4.1E-02 1
rs1786814
CELF4
18 37497065 intron variant G/A;C snv 1
rs1568523935
SLC25A42
0.776 0.240 19 19105656 stop gained C/G snv 20
rs766265889
TTN-AS1 ; TTN
0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs114638163
MIPEP
0.827 0.240 13 23805994 stop gained C/A;T snv 4.0E-06; 1.3E-03 10
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs397516955
DSP
0.790 0.120 6 7562753 stop gained G/A snv 9
rs201217593
DMD
0.790 0.200 X 31177947 stop gained C/T snv 2.2E-05 2.9E-05 8
rs1057518422
TAB2
0.851 0.240 6 149378954 stop gained C/T snv 7
rs397516915
DSP
0.925 0.080 6 7568443 stop gained C/T snv 4.0E-06 6
rs397517689
TTN-AS1 ; TTN
0.882 0.160 2 178574530 stop gained G/A snv 4.0E-06 5
rs56816490
LMNA
0.925 0.120 1 156135913 stop gained G/A;T snv 4
rs72646846
TTN ; TTN-AS1
0.925 0.160 2 178589849 stop gained G/A snv 7.6E-05 6.3E-05 4
rs1242465339
UQCRFS1
1.000 0.080 19 29207763 stop gained G/A;T snv 7.0E-06 3
rs1553644307
TTN ; TTN-AS1
0.925 0.160 2 178591418 stop gained T/A snv 3
rs267607554
LMNA
1.000 0.080 1 156135925 stop gained C/T snv 3
rs28763965
DSP
0.925 0.120 6 7580562 stop gained C/A;G;T snv 8.0E-06; 1.7E-03; 4.0E-06 3
rs371678190
TTN-AS1 ; TTN
1.000 0.040 2 178578066 stop gained G/A;T snv 4.0E-06; 5.6E-05 3
rs727504289
MYBPC3
0.925 0.080 11 47332932 stop gained G/A;T snv 8.3E-06; 4.1E-06 3
rs1425855043
PKP2
1.000 0.080 12 32878105 stop gained C/A snv 2