Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs672601334
RIT1
0.752 0.400 1 155904798 missense variant G/C snv 18
rs730881014
RIT1
0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 9
rs121964856
TNNT2
0.807 0.120 1 201365297 missense variant C/A;T snv 8
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs1057517686
ATAD3A
0.827 0.120 1 1529299 missense variant C/T snv 7
rs45586240
TNNT2
0.827 0.080 1 201361989 missense variant G/A;T snv 4.0E-06 7
rs121964858
TNNT2
0.807 0.120 1 201365244 missense variant A/C;G;T snv 6
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 6
rs397516456
TNNT2
0.827 0.080 1 201365298 missense variant G/A snv 4.0E-06 1.4E-05 5
rs56657623
LMNA
0.827 0.120 1 156138540 missense variant G/A snv 1.6E-05 7.0E-06 5
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 5
rs727504246
TNNT2
0.827 0.080 1 201363330 missense variant G/A snv 5
rs727504247
TNNT2
0.827 0.080 1 201359217 stop gained C/A;T snv 4.1E-06 7.0E-06 5
rs121964855
TNNT2
0.851 0.080 1 201365638 missense variant A/T snv 4.0E-06 4
rs121964857
TNNT2
0.851 0.080 1 201359245 missense variant G/A snv 3.6E-04 4.3E-04 4
rs200754249
TNNT2
0.851 0.080 1 201368212 missense variant G/A;T snv 4.5E-04; 4.0E-06 4
rs397516455
TNNT2
0.851 0.080 1 201365617 missense variant T/G snv 4.0E-06 7.0E-06 4
rs397516457
TNNT2
0.851 0.080 1 201365291 missense variant C/A;T snv 4
rs397516463
TNNT2
0.851 0.080 1 201364369 missense variant G/A snv 1.4E-05 4
rs397516470
TNNT2
0.851 0.080 1 201363377 inframe deletion CTC/- delins 4
rs730881116
TNNT2
0.851 0.080 1 201359216 stop gained C/T snv 4
rs727502886
ACTN2
0.925 0.040 1 236719007 missense variant G/A snv 3
rs730881098
TNNT2
0.882 0.040 1 201365613 missense variant A/C snv 3