Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv 8
rs121909775
CASP10
1.000 0.120 2 201205929 stop gained C/A;T snv 4.0E-06 2
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs63750042
MSH2
0.925 0.240 2 47408415 stop gained C/G;T snv 4.0E-06 6
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs3749474
TMEM165 ; CLOCK
0.724 0.320 4 55434518 3 prime UTR variant C/T snv 0.33 17
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs28936699
CASP10
1.000 0.120 2 201209388 missense variant C/T snv 1
rs1979277
SHMT1
0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 45
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
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 16
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs398122820
B2M
0.790 0.240 15 44715641 missense variant G/A snv 8