Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 7
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 7
rs1239905891
IGF1
0.925 0.080 12 102475786 missense variant G/A;T snv 3
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs730881360
ATM
11 108227629 missense variant G/A;C snv 1
rs1555114766
C11orf65 ; ATM
11 108317486 stop gained G/A snv 1
rs28904921
C11orf65 ; ATM
0.763 0.320 11 108329202 missense variant T/G snv 4.0E-05 6.3E-05 12
rs1057519915
MTOR
0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519916
MTOR
0.882 0.160 1 11109320 missense variant T/A snv 4
rs1057519913
MTOR
0.925 0.120 1 11157172 missense variant G/C snv 3
rs786205165
MTOR
0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519914
MTOR
0.851 0.240 1 11157174 missense variant A/G snv 5
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 7
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1302103336
CHEK1
0.776 0.120 11 125637491 missense variant T/C snv 8.1E-06 12
rs1057519943
POLE
0.790 0.160 12 132676598 missense variant G/C;T snv 10