Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs1799821
CPT2
0.827 0.200 1 53210776 missense variant G/A snv 0.49 0.46 8
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs45586240
TNNT2
0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 7
rs202101384
SDHB
0.851 0.160 1 17044818 missense variant T/A snv 4.4E-05 1.4E-05 6
rs4641
LMNA
0.851 0.120 1 156137743 splice region variant C/T snv 0.26 0.21 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs59270054
LMNA
0.925 0.120 1 156115162 missense variant G/A;C snv 6
rs397516484
TNNT2
0.851 0.080 1 201359244 missense variant C/G;T snv 1.2E-05 5
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs74315293
CPT2
0.851 0.200 1 53213509 missense variant C/T snv 2.4E-05 1.4E-05 5
rs863225119
TNNT2
0.882 0.080 1 201359632 missense variant T/A snv 5
rs1799822
CPT2
0.925 0.080 1 53213557 missense variant A/G snv 0.16 0.15 4
rs267607571
LMNA
0.882 0.160 1 156134458 missense variant G/A;T snv 4
rs56816490
LMNA
0.925 0.120 1 156135913 stop gained G/A;T snv 4
rs59301204
LMNA
0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs74315323
HJV
0.882 0.080 1 146018399 missense variant C/A snv 1.7E-04 2.7E-04 4
rs1057518905
DPM3
1 155140104 missense variant A/T snv 3
rs10927875
ZBTB17
1.000 0.040 1 15972817 intron variant C/T snv 0.29 3
rs267607554
LMNA
1.000 0.080 1 156135925 stop gained C/T snv 3
rs371792178
DPYD
0.925 0.040 1 97699507 missense variant G/A;C snv 3.6E-05; 1.2E-05 3
rs587777425
DCAF8
1.000 1 160237145 missense variant G/A;T snv 3