Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1568523935
SLC25A42
0.776 0.240 19 19105656 stop gained C/G snv 20
rs104894201
CRYAB
0.763 0.280 11 111908934 missense variant T/C snv 12
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs121918312
BAG3
0.776 0.160 10 119672373 missense variant C/A;T snv 11
rs104894369
MYL2
0.807 0.080 12 110914287 missense variant C/A;T snv 10
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs121913628
MYH7
0.763 0.160 14 23424059 missense variant C/G;T snv 10
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv 10
rs3218713
MYH7
0.763 0.160 14 23431468 missense variant C/A;T snv 10
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv 9
rs397516955
DSP
0.790 0.120 6 7562753 stop gained G/A snv 9
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs1057518422
TAB2
0.851 0.240 6 149378954 stop gained C/T snv 7
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv 6
rs1555661648
AQP4 ; AQP4-AS1
0.882 0.240 18 26862297 missense variant C/G snv 6
rs267607490
DES
0.925 0.160 2 219425734 missense variant C/T snv 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
rs104893823
TNNC1
0.882 0.040 3 52451285 missense variant C/T snv 5