Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786204195
CDKN2A
0.851 0.200 9 21974686 missense variant G/A;T snv 4
rs786203926
ATM
0.882 0.120 11 108227678 synonymous variant T/C snv 4
rs78417682
TNS3
0.925 0.120 7 47449305 intron variant G/C snv 0.15 2
rs78303930
NES
0.925 0.120 1 156670593 missense variant C/A;G snv 4.0E-06; 2.4E-03 4
rs782128510
C17orf97 ; LOC105371430
0.925 0.120 17 410373 missense variant C/A;G snv 7.6E-05; 8.4E-06 2
rs782095550
MANF
0.925 0.120 3 51386267 missense variant T/C snv 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs779731636
SOD2
0.925 0.120 6 159685026 missense variant C/A snv 8.6E-06 2
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs767964519
NFE2L2
0.925 0.120 2 177231869 missense variant T/C snv 4.0E-06 2
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs766333007
MUC1
0.776 0.280 1 155192274 missense variant C/T snv 7.0E-06 8
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs762581936
MUC4
0.827 0.240 3 195788569 missense variant C/G;T snv 1.1E-05; 1.1E-05 5
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs757748401
NFATC2
0.925 0.120 20 51542465 missense variant C/A;T snv 5.2E-06 3
rs752967378
RAF1
0.882 0.160 3 12618580 missense variant G/A;C snv 4.0E-06 3
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 3
rs747601652
CRYZ
0.925 0.120 1 74723233 missense variant A/G snv 1.2E-05 2
rs74315364
RNASEL
0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs72552266
CYP2A13
0.882 0.200 19 41089049 stop gained C/G;T snv 4.0E-06; 5.8E-03 3
rs7164773
RORA
0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs7106914
SBF2
1.000 0.120 11 9956424 intron variant T/C snv 0.38 1
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2