Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs145204276
ZBTB37 ; SNORD74 ; SNORD75 ; GAS5 ; SNORD77 ; SNORA103 ; SNORD76
0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23