Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852973
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 13
rs137852972
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 9
rs58932704
LMNA
0.776 0.200 1 156136413 missense variant C/T snv 8
rs879254764
LDLR
0.827 0.360 19 11110752 frameshift variant G/- delins 7
rs563539429
AGPAT2
0.851 0.240 9 136677540 missense variant C/A;G;T snv 4.1E-06; 8.1E-06; 1.5E-03 5
rs137852975
HNRNPUL2-BSCL2 ; BSCL2
0.851 0.240 11 62692671 stop gained C/A snv 2.0E-05 1.4E-05 5
rs587783668
KCNJ11
0.882 0.240 11 17387629 missense variant C/T snv 1.2E-05 4
rs267607619
LMNA
0.882 0.160 1 156130666 missense variant G/C snv 3
rs267607639
LMNA
0.882 0.200 1 156136939 missense variant T/C snv 3
rs121908093
ZMPSTE24
0.882 0.160 1 40285988 missense variant T/C snv 3
rs606231168
AGPAT2
0.925 0.120 9 136676681 splice acceptor variant C/G snv 4.0E-06 7.0E-06 2
rs764260414
AGPAT2
0.925 0.120 9 136677440 missense variant C/T snv 8.0E-06 1.4E-05 2
rs121434501
CAV1
0.925 0.120 7 116526606 stop gained G/T snv 4.0E-06 7.0E-06 2
rs1064797076
HNRNPUL2-BSCL2 ; BSCL2
1.000 0.120 11 62692385 frameshift variant AAGTGCGCGTG/- delins 1