Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
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
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs522616
MMP3
0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 10
rs11545664
ENG
0.925 0.120 9 127843106 synonymous variant C/T snv 9.3E-02 0.14 4
rs201393380
LOC105379841 ; ENG
0.925 0.120 9 127825767 missense variant C/G snv 1.3E-04 7.8E-04 4
rs897009059
RAF1
0.925 0.120 3 12618557 missense variant G/C snv 4.0E-06 2
rs9509
SLC12A5-AS1 ; MMP9
0.925 0.120 20 46016514 3 prime UTR variant T/C snv 0.11 2