Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4733220
WRN
0.807 0.120 8 31043374 intron variant A/G snv 0.50 6
rs587778872
CRYGC ; LOC100507443
0.807 0.200 2 208128231 missense variant G/A;C snv 8.0E-06 6
rs727502810
RIC3 ; TUB
0.827 0.160 11 8100575 frameshift variant AGAG/-;AG delins 8
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs104893736
CRYGS
0.827 0.040 3 186539566 missense variant C/A snv 5
rs1050829
G6PD
0.827 0.160 X 154535277 missense variant T/A;C snv 1.7E-04; 2.6E-02 5
rs387907338
HSPB2-C11orf52 ; HSPB2 ; CRYAB
0.827 0.200 11 111911559 missense variant G/A;T snv 5
rs79121622
HSF4
0.827 0.080 16 67165833 missense variant G/A snv 3.3E-04 9.8E-05 5
rs1554781700
COL5A1
0.851 0.240 9 134701287 missense variant G/T snv 12
rs1423415130
XYLT2
0.851 0.120 17 50360241 missense variant G/A snv 7.0E-06 6
rs143810759
LIG4
0.851 0.280 13 108210371 missense variant C/T snv 1.6E-04 2.1E-04 6
rs80338829
MYH9
0.851 0.200 22 36295069 missense variant G/A snv 5
rs8702
KLC1
0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs1114167307
GJA3
0.851 0.200 13 20143233 missense variant G/A snv 4
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
rs150857132
CRYGD ; LOC100507443
0.851 0.200 2 208124183 missense variant C/A;T snv 4.4E-04; 4.0E-06 4
rs398122944
LOC100507443 ; CRYGC
0.851 0.200 2 208128257 stop gained C/G;T snv 4
rs778791846
SMO
0.851 0.200 7 129210515 missense variant C/T snv 2.0E-05 4
rs1057518802
SLC19A1 ; COL18A1
0.882 0.080 21 45509554 stop gained C/T snv 4
rs1303044966
ABHD12
0.882 0.160 20 25339294 stop gained G/A;C snv 4.0E-06 4
rs141638421
CRYAB
0.882 0.080 11 111908822 missense variant C/T snv 7.2E-05 4.9E-05 4
rs387907339
CRYAB
0.882 0.280 11 111908967 missense variant C/A;G snv 4