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
rs1555257073
POMP
0.827 0.120 13 28672407 frameshift variant AT/- delins 25
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs28931594
GJB2
0.790 0.280 13 20189434 missense variant C/A;T snv 9
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 8
rs1482518887
RUNX1
0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs1555119899
ATM ; C11orf65
0.925 0.240 11 108326149 missense variant G/C snv 7
rs1555908409
RAC2
0.851 0.160 22 37232842 missense variant C/T snv 7
rs1057518965
ATM
0.882 0.320 11 108244812 frameshift variant A/- delins 5
rs128620185
BTK
0.882 0.240 X 101375202 missense variant C/T snv 4
rs2227513
LOC105369818 ; IL22
1.000 0.080 12 68253559 intron variant T/C snv 0.15 3
rs128621195
BTK
1.000 0.120 X 101358672 missense variant T/C snv 2
rs746540053
CD34 ; LOC107985253
1.000 0.040 1 207911034 missense variant C/T snv 2
rs1336343565
RAG1 ; RAG2 ; IFTAP
11 36592848 missense variant G/T snv 7.0E-06 1
rs2204985
LOC105370401
14 22448641 intron variant G/A snv 0.52 1
rs3218716
MYH7
0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 17
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs1188975135
APOBEC3C ; APOBEC3F
0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs201137953
DPP4
2 162039019 missense variant T/A;C snv 4.0E-06 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs778036161
RUNX1T1
0.776 0.080 8 92017363 missense variant T/C snv 8.0E-06 9
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57