Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs765019311
AVP
0.925 0.040 20 3082716 missense variant C/A;G;T snv 2
rs377423839
BFSP2
0.925 0.080 3 133400418 missense variant G/A snv 5.2E-05 1.4E-05 2
rs930526408
BFSP2 ; BFSP2-AS1
0.925 0.040 3 133472412 missense variant G/A;T snv 2
rs118203965
CHMP4B
0.925 0.040 20 33850969 missense variant A/T snv 2
rs1250875000
CRYAA2 ; LOC102724843 ; LOC102724701
0.925 0.040 21 6560927 missense variant C/A;T snv 2
rs1227057051
CRYAA ; LOC107987300
1.000 0.040 21 43172266 missense variant G/A snv 8.2E-06 2
rs139750142
CRYAB
0.925 0.200 11 111910446 missense variant G/A;T snv 9.5E-05; 4.0E-06 6.3E-05 2
rs375933774
CRYAB ; HSPB2-C11orf52 ; HSPB2
0.925 0.040 11 111911691 missense variant G/A snv 2.3E-05 3.5E-05 2
rs140372256
CRYGA
0.925 0.040 2 208160859 stop gained C/A;G;T snv 1.5E-04; 1.6E-05; 4.0E-06 2
rs750872744
CRYGC ; LOC100507443
0.925 0.040 2 208128325 stop gained C/A;T snv 3.6E-05 2
rs1483130765
CRYGS
0.925 0.040 3 186538833 stop gained C/A snv 7.0E-06 2
rs139787163
EPHA2
0.925 0.120 1 16125271 missense variant C/T snv 4.8E-04 3.6E-04 2
rs3754334
EPHA2
0.925 0.040 1 16125272 synonymous variant G/A snv 0.28 0.24 2
rs777441702
GCNT2
0.925 0.080 6 10621360 missense variant G/A snv 1.2E-05 1.4E-05 2
rs1215029143
IKBKG
1.000 0.040 X 154558608 missense variant G/A;T snv 2
rs746066696
IPO13
0.925 0.080 1 43949663 missense variant C/T snv 8.0E-06 7.0E-06 2
rs8007903
KLC1
0.925 0.120 14 103671306 intron variant A/G snv 0.27 2
rs1568480054
LIM2
0.925 0.200 19 51380577 missense variant G/A snv 2
rs61751949
LOC100507443 ; CRYGC
0.925 0.200 2 208129550 missense variant C/T snv 1.7E-02 1.1E-02 2
rs727502768
LOC101928230 ; MAF
0.925 0.240 16 79599697 missense variant G/C snv 2
rs121917867
MIP
0.925 0.040 12 56453703 missense variant G/A;C snv 4.0E-05 2
rs761738142
NOL3 ; HSF4
0.925 0.200 16 67169060 stop gained C/A;T snv 8.0E-06; 4.0E-06 2
rs11129182
RARB
0.925 0.120 3 25129806 intron variant T/C snv 0.82 2
rs375713569
SDS
0.925 0.040 12 113398748 missense variant G/A;C snv 3.6E-05; 1.2E-05 2
rs17047586
TAFA1
0.925 0.120 3 68363724 intron variant A/G snv 8.6E-03 2