Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs367543041
TARDBP
0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs80356730
TARDBP
0.807 0.120 1 11022418 missense variant A/G snv 8.0E-06 7
rs80356733
TARDBP
0.790 0.200 1 11022451 missense variant G/T snv 7
rs4884357
TARDBP
0.807 0.120 1 11022301 missense variant G/A;T snv 4.0E-06 6
rs80356715
TARDBP
0.807 0.120 1 11016874 missense variant C/G;T snv 8.0E-06; 2.2E-04 6
rs2412208
CAMTA1
0.827 0.080 1 7032722 intron variant T/G snv 0.33 5
rs267607102
TARDBP
0.851 0.120 1 11022196 missense variant A/G snv 5
rs80356717
TARDBP
0.851 0.120 1 11018836 missense variant A/G snv 5
rs80356718
TARDBP
0.827 0.120 1 11022209 missense variant A/G snv 7.6E-05 4.9E-05 5
rs80356734
TARDBP
0.851 0.160 1 11022464 missense variant A/G snv 4
rs12136973
KIAA0040
1.000 0.080 1 175171183 intron variant T/C snv 0.22 3
rs1541160
KIFAP3
0.882 0.080 1 170026661 intron variant C/A;T snv 3
rs771845093
MFN2
0.925 0.160 1 12005903 missense variant G/A snv 8.0E-06 7.0E-06 3
rs80356719
TARDBP
0.882 0.080 1 11022268 missense variant G/A;C snv 1.6E-05 3
rs80356727
TARDBP
0.925 0.080 1 11022400 missense variant C/A snv 3
rs121908395
TARDBP
0.925 0.080 1 11022278 missense variant G/C;T snv 2
rs1572931
RAB29 ; LOC105371702
0.925 0.080 1 205775090 splice region variant C/A;T snv 0.14 2
rs376557198
ZNF436
0.925 0.080 1 23363034 missense variant G/C snv 8.0E-06 2
rs6703183
LOC105372898
0.925 0.080 1 209539544 intron variant T/C snv 0.48 2
rs797044594
TARDBP
0.925 0.080 1 11022559 missense variant G/C snv 2
rs80356721
TARDBP
0.925 0.080 1 11022290 missense variant G/A;C;T snv 4.0E-06; 1.2E-05 2
rs80356732
TARDBP
0.925 0.080 1 11022444 missense variant C/A snv 8.0E-06 2
rs80356738
TARDBP
0.925 0.080 1 11022544 missense variant T/C;G snv 2