Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912678
ACVR1
0.851 0.080 2 157774114 missense variant C/G;T snv 8
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 14
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs587777108
ATL3 ; LOC107984336
0.925 0.080 11 63646550 missense variant T/C snv 5
rs80338852
B3GLCT
0.925 0.200 13 31317599 stop gained T/A;C snv 8.0E-06 3
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs12720071
CNR1
0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs1234344050
COL3A1 ; LOC105373791
2 188984825 missense variant C/G snv 4.0E-06 2
rs387906617
CREB1
2 207567506 missense variant A/G snv 2
rs79204362
CYP1B1
0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 10
rs57865060
CYP1B1-AS1 ; CYP1B1
0.827 0.160 2 38074704 missense variant C/T snv 1.1E-02 5.7E-03 6
rs201968272
DDX11
0.925 0.160 12 31089147 missense variant G/A snv 3
rs201405525
DECR1
0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3
rs764120087
EP300
22 41117439 missense variant G/A snv 8.0E-06 2
rs7650466
EPHA3
0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs137854438
FAM83H
1.000 0.080 8 143728570 stop gained A/T snv 2
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1057519320
FBN1
0.807 0.160 15 48444574 missense variant G/A snv 7
rs1057519321
FBN2
0.807 0.160 5 128349391 missense variant C/A;T snv 7
rs142322800
FCGR3A
1 161548502 missense variant T/C snv 1.5E-04 5.6E-05 1
rs1206736425
FCGR3B
1 161626229 missense variant T/C snv 2
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 28
rs121918502
FGFR2
0.790 0.160 10 121517351 missense variant G/C snv 9
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31