Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs351365
WNT2B
1.000 0.120 1 112503773 intron variant T/C;G snv 1
rs6662005
ERO1B
1.000 0.120 1 236276616 intron variant G/A snv 0.16 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs4668123
LRP2
0.851 0.280 2 169196995 missense variant C/A;G;T snv 6
rs2229629
HK2
0.882 0.120 2 74889400 missense variant G/A snv 6.0E-02 0.18 4
rs63751412
MSH2
0.882 0.200 2 47429869 stop gained C/A;G;T snv 8.0E-06; 4.0E-06 4
rs980303898
LOC101929532 ; GCG
0.851 0.120 2 162147479 missense variant T/C snv 8.0E-06 7.0E-06 4
rs145733073
UGT1A8 ; UGT1A9 ; UGT1A7 ; UGT1A10
0.925 0.120 2 233682175 missense variant T/C;G snv 4.0E-06; 1.4E-04 2
rs767964519
NFE2L2
0.925 0.120 2 177231869 missense variant T/C snv 4.0E-06 2
rs876661110
FBXO11 ; MSH6
0.925 0.120 2 47791093 missense variant G/A snv 2
rs12478462 1.000 0.120 2 152798206 intergenic variant T/G snv 0.28 1
rs12620038
EPCAM-DT
1.000 0.120 2 47248996 intron variant C/G;T snv 1
rs1486134 1.000 0.120 2 67412637 downstream gene variant G/C;T snv 1
rs962856
LINC01829
1.000 0.120 2 67366671 intron variant C/T snv 0.66 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131