Disease: Congestive heart failure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10927887
CLCNKA
0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs121918598
RYR2
0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs1253810269
ARID1A
0.882 0.080 1 26696971 missense variant G/A snv 7.0E-06 3
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs3766871
RYR2
0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs567798234
AMPD2
0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
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
rs61661343
LMNA
0.851 0.040 1 156130687 missense variant T/C snv 4
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs749303395
AMPD1
0.882 0.040 1 114680329 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs10932374
ERBB4
0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs13003941
ERBB4
0.925 0.040 2 211378978 3 prime UTR variant G/C;T snv 0.26 2
rs1595064
ERBB4
0.925 0.040 2 211378020 3 prime UTR variant G/A;C snv 2
rs1595065
ERBB4
0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2
rs267607499
DES
0.851 0.160 2 219418809 missense variant A/G;T snv 4
rs3748960
ERBB4
0.925 0.040 2 211383109 3 prime UTR variant C/T snv 0.96 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131