Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801271
CSF1R
5 150054082 missense variant T/A;C snv 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs2285489
ADAMTS13
9 133424254 intron variant T/C snv 0.68 2
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs777017502
CEBPZ
0.925 0.080 2 37222420 missense variant T/C;G snv 4.2E-06; 4.2E-06 3
rs387906664
CBL
1.000 11 119278220 missense variant T/C;G snv 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8