Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800023
CCR5 ; CCR5AS
1.000 0.040 3 46370817 intron variant A/G snv 0.29 2
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1801271
CSF1R
5 150054082 missense variant T/A;C snv 2
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs2239704
LTA ; LOC100287329
0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs2285489
ADAMTS13
9 133424254 intron variant T/C snv 0.68 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs267606706
CBL
0.807 0.240 11 119278181 missense variant T/A;C snv 8.0E-06 9
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs387906664
CBL
1.000 11 119278220 missense variant T/C;G snv 2
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs397507514
PTPN11
0.790 0.240 12 112450408 missense variant G/C;T snv 10
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs724159945
ETV6
1.000 12 11885968 missense variant C/A;T snv 3
rs724159946
ETV6
1.000 12 11884541 missense variant G/A snv 7.0E-06 3
rs724159947
ETV6
0.851 0.120 12 11869601 missense variant C/T snv 6
rs757333753
RAF1
0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 6
rs757874631
CBL
0.882 0.120 11 119278211 missense variant T/A;C snv 4
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8