Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs765545512
HFE
0.827 0.240 6 26093226 missense variant G/A;T snv 4.0E-06; 1.6E-05 6
rs1559279177
HJV
0.851 0.160 1 146018661 frameshift variant G/- del 5
rs56793579
LMNA
0.851 0.240 1 156115102 missense variant C/G;T snv 5
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs13058338
RAC2
1.000 0.040 22 37236730 intron variant T/A;G snv 4
rs1553265736
LMNA
0.925 0.040 1 156136080 missense variant G/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
rs587782927
DSP
0.882 0.080 6 7574084 splice region variant AG/- delins 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
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
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
rs794728602
LMNA
1.000 0.040 1 156115168 missense variant G/A snv 3
rs899115126
EDNRA
0.882 0.080 4 147542603 missense variant G/C snv 3
rs1337916669
LOC108783645 ; HFE
0.925 0.040 6 26092879 missense variant G/T snv 2
rs1429117513
LAG3
0.925 0.040 12 6775316 synonymous variant T/C snv 4.0E-06 2
rs1595064
ERBB4
0.925 0.040 2 211378020 3 prime UTR variant G/A;C snv 2