Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121917869
MIP
0.851 0.080 12 56453715 missense variant T/C;G snv 4
rs137853924
LOC100507443 ; CRYGC
0.851 0.200 2 208128343 missense variant C/A;T snv 4
rs1463326176
LOC100507443 ; CRYGD
0.851 0.200 2 208124291 frameshift variant TGGG/- del 4
rs387907339
CRYAB
0.882 0.280 11 111908967 missense variant C/A;G snv 4
rs398122944
LOC100507443 ; CRYGC
0.851 0.200 2 208128257 stop gained C/G;T snv 4
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs118203966
CHMP4B
0.882 0.040 20 33851064 missense variant G/A snv 3
rs121909595
LOC100507443 ; CRYGD
0.925 0.040 2 208124321 missense variant G/A snv 3
rs121909596
LOC100507443 ; CRYGD
0.925 0.040 2 208124188 missense variant C/T snv 3
rs121912973
CRYAA ; LOC107987300
0.882 0.040 21 43172105 missense variant G/A snv 3
rs17175798
ANKRD34C-AS1
0.925 0.040 15 79171618 intron variant C/A;T snv 3
rs2101521
TLR1
0.925 0.080 4 38809930 intron variant G/A;T snv 3
rs398122937
GJA3
0.882 0.040 13 20142862 missense variant C/T snv 3
rs398122947
LOC107987300 ; CRYAA
0.882 0.040 21 43170619 missense variant G/A snv 3
rs587783070
IARS2
0.925 0.040 1 220143109 missense variant C/T snv 3
rs644242
PAX6
0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 3
rs864309688
GJA8
0.882 0.200 1 147908089 missense variant G/C snv 7.0E-06 3
rs11129182
RARB
0.925 0.120 3 25129806 intron variant T/C snv 0.82 2
rs118203965
CHMP4B
0.925 0.040 20 33850969 missense variant A/T snv 2
rs1215029143
IKBKG
1.000 0.040 X 154558608 missense variant G/A;T snv 2
rs1250875000
CRYAA2 ; LOC102724843 ; LOC102724701
0.925 0.040 21 6560927 missense variant C/A;T snv 2
rs1483130765
CRYGS
0.925 0.040 3 186538833 stop gained C/A snv 7.0E-06 2
rs1568480054
LIM2
0.925 0.200 19 51380577 missense variant G/A snv 2
rs17047586
TAFA1
0.925 0.120 3 68363724 intron variant A/G snv 8.6E-03 2