Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs7081476
ANKRD26
0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 6
rs371401403
MYBPC3
0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs397516089
MYH7
0.827 0.080 14 23429807 missense variant C/G;T snv 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs587782951
JPH2
0.807 0.080 20 44160305 missense variant G/T snv 6
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs267607499
DES
0.851 0.160 2 219418809 missense variant A/G;T snv 4
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4
rs10927887
CLCNKA
0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs12362161 1.000 0.040 11 98834502 intergenic variant C/A;G snv 3
rs1258130495
EDNRA
0.882 0.040 4 147485727 missense variant G/A snv 3
rs1303946678
CYP2D6 ; NDUFA6-DT
0.925 0.040 22 42126851 missense variant C/G snv 3
rs189919070
MIR4788
1.000 0.040 3 134436825 upstream gene variant C/A;T snv 3
rs200536955
HSPB6 ; PROSER3
0.925 0.040 19 35756980 missense variant G/A;T snv 7.0E-04 3
rs3829365
POSTN
0.925 0.040 13 37598759 5 prime UTR variant G/A;C snv 4.0E-06; 0.11 3
rs749303395
AMPD1
0.882 0.040 1 114680329 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs7965830
LOC105369844
1.000 0.040 12 75962050 intron variant C/A;T snv 3
rs79661299 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 3