Disease: Cardiomyopathy, Familial Idiopathic
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1805124
SCN5A
0.742 0.280 3 38603929 missense variant T/C snv 0.22 0.25 16
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 15
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 11
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs121913002
DES
0.851 0.160 2 219425727 missense variant C/A;G;T snv 6.5E-05; 5.6E-04 7
rs150821281
PKP2
0.827 0.080 12 32878461 missense variant G/A snv 2.3E-03 2.5E-03 7
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 7
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs199476301
TPM1
0.851 0.040 15 63042874 missense variant G/A;T snv 4.0E-06 6
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 6
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
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 6
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 6
rs104893823
TNNC1
0.882 0.040 3 52451285 missense variant C/T snv 5
rs104894501
TPM1
0.851 0.040 15 63044030 stop gained G/A;C;T snv 4.0E-06 5
rs121917776
VCL
0.882 0.040 10 74112086 missense variant C/T snv 9.9E-05 7.0E-06 5
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 5