Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 8
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs9485372
TAB2
0.807 0.120 6 149287738 intron variant G/A snv 0.20 6
rs2288349
DNMT1
0.882 0.120 19 10146569 intron variant G/A snv 0.36 0.35 5
rs12662670
CCDC170
0.851 0.080 6 151597721 intron variant T/C;G snv 4
rs1436904
AQP4-AS1 ; CHST9
0.851 0.080 18 26990703 intron variant T/G snv 0.35 4
rs40239
MET
0.851 0.120 7 116677823 intron variant G/A snv 0.87 4
rs527616
AQP4-AS1
0.851 0.080 18 26757460 intron variant C/G snv 0.71 4
rs10274701
EZH2
0.925 0.080 7 148855364 intron variant C/T snv 0.76 2
rs1651654
C16orf87
0.925 0.080 16 46822677 intron variant T/C snv 0.79 2
rs2278256
USHBP1 ; BABAM1
0.925 0.080 19 17267350 intron variant T/C snv 0.23 2
rs635538
LOC105372126 ; TCF4
0.925 0.080 18 55606383 intron variant G/A snv 0.94 2
rs7250266
BABAM1 ; USHBP1
0.925 0.080 19 17266803 intron variant C/G snv 8.5E-02 2
rs80350973
LOC730100
0.925 0.080 2 52252219 intron variant A/T snv 2.1E-05 2
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 7
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 5
rs718282 0.925 0.080 7 152638744 intergenic variant A/G snv 0.94 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986
CD3EAP ; ERCC1
0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42