Disease: Cardiomyopathy, Familial Idiopathic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199476314
TPM1
0.882 0.040 15 63060930 missense variant T/G snv 4
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 6
rs2234962
BAG3
1.000 0.040 10 119670121 missense variant T/C snv 0.17 0.15 3
rs267607155
TTN
0.925 0.040 2 178782980 missense variant A/G;T snv 3
rs267607578
LMNA
0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 3
rs28933090
LMNA
0.925 0.160 1 156115172 missense variant T/A;G snv 3
rs28933091
LMNA
0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs28933092
LMNA
1.000 0.040 1 156134497 missense variant A/G;T snv 2
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs397516607
RBM20
0.925 0.040 10 110821356 missense variant G/A snv 4
rs397516695
DES
0.882 0.040 2 219418869 missense variant T/A;C snv 5.5E-05 4
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs397517889
LMNA
0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 3
rs41310765
SCN5A
0.882 0.120 3 38575424 missense variant G/A snv 1.4E-04 7.7E-05 5
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs535039125
CYP2B6
0.851 0.040 19 41004380 missense variant C/T snv 1.1E-04 1.3E-04 5
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs57045855
LMNA
0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs59301204
LMNA
0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 4
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134