Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 23
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs7538876
PADI6
0.807 0.120 1 17395867 intron variant G/A snv 0.37 5
rs157935
LINC00513 ; LINC-PINT
0.851 0.040 7 130900794 intron variant T/G snv 0.28 4
rs16917546
LOC105378327 ; ZNF365
0.851 0.040 10 62637778 intron variant T/C snv 0.29 4
rs214782
TGM3 ; LOC105372503
0.851 0.040 20 2301324 intron variant G/A snv 0.73 4
rs59586681 0.851 0.040 20 2239664 intron variant A/G;T snv 0.34 4
rs7006527
RGS22
0.851 0.040 8 100012277 intron variant A/C;T snv 4
rs12202284
LOC105374875
0.925 0.080 6 471136 intron variant C/A;T snv 3
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 1
rs775248597
ATM
0.851 0.120 11 108229185 stop gained C/G;T snv 8.1E-06 5
rs786203714
PALB2
0.925 0.200 16 23635095 stop gained A/T snv 4
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs1126809
LOC107984363 ; TYR
0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 20
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 16
rs879255280
SMO
0.701 0.200 7 129206557 missense variant C/T snv 15
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 13
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 9
rs1800407
OCA2
0.807 0.200 15 27985172 missense variant C/T snv 4.7E-02 4.9E-02 5
rs214803
TGM3
0.851 0.040 20 2309687 missense variant C/A;G;T snv 0.82; 4.0E-06 4
rs3769823
CASP8
0.851 0.040 2 201258272 missense variant A/G snv 0.66 0.65 4
rs11170164
KRT5
0.827 0.120 12 52519884 missense variant C/T snv 5.7E-02 5.3E-02 3
rs13014235
FLACC1
0.851 0.040 2 201350769 missense variant C/G snv 0.62 0.63 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3