Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786205186
FLNA
0.827 0.120 X 154362417 splice donor variant C/G;T snv 5
rs1557178535
FLNA
0.851 0.120 X 154363633 intron variant A/T snv 4
rs1557179325
FLNA
0.925 0.080 X 154366562 splice region variant C/T snv 4
rs137853310
FLNA
0.925 0.080 X 154367920 stop gained G/A snv 2
rs398122812
LOC105373386 ; FLNA
0.925 0.080 X 154348897 stop gained C/T snv 2
rs1554054827
MAP1B
1.000 0.080 5 72194173 frameshift variant C/- delins 1
rs1554054831
MAP1B
1.000 0.080 5 72194262 stop gained C/T snv 1
rs1554054880
MAP1B
1.000 0.080 5 72194949 stop gained C/T snv 1
rs1554055106
MAP1B
1.000 0.080 5 72196671 stop gained C/T snv 1
rs398123620
FLNA
1.000 0.080 X 154359010 frameshift variant -/AT delins 1
rs786205177
FLNA
1.000 0.080 X 154365487 splice acceptor variant C/A snv 1
rs786205178
FLNA
1.000 0.080 X 154352312 frameshift variant ACTG/- delins 1
rs786205180
FLNA
1.000 0.080 X 154366562 frameshift variant CTTAT/- del 1
rs786205181
FLNA
1.000 0.080 X 154371109 frameshift variant T/- del 1
rs786205182
FLNA
1.000 0.080 X 154364927 stop gained A/T snv 1
rs786205183
FLNA
1.000 0.080 X 154364721 splice acceptor variant T/C snv 1
rs786205188
FLNA
1.000 0.080 X 154360266 frameshift variant C/- delins 1
rs786205189
FLNA
1.000 0.080 X 154359822 frameshift variant -/ACGGGCCTTGACGT delins 1
rs786205190
FLNA
1.000 0.080 X 154359635 coding sequence variant -/TCCTGGAGGAGTGCAG delins 1
rs786205191
FLNA
1.000 0.080 X 154359620 frameshift variant C/- del 1
rs786205194
FLNA
1.000 0.080 X 154358336 frameshift variant GC/- del 1
rs786205197
FLNA
1.000 0.080 X 154357444 stop gained G/T snv 1
rs786205198
FLNA
1.000 0.080 X 154357436 frameshift variant G/- del 1
rs786205199
FLNA
1.000 0.080 X 154355020 frameshift variant CA/- delins 1
rs786205201
FLNA
1.000 0.080 X 154352795 frameshift variant TT/- del 1