Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1239105602
PTEN ; KLLN
1.000 0.160 10 87864168 5 prime UTR variant C/T snv 2
rs917927904
PTEN ; KLLN
1.000 0.160 10 87864242 5 prime UTR variant G/T snv 7.0E-06 2
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
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
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
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
rs1057519802
CSF1R
5 150061765 missense variant A/C snv 2
rs121913390
CSF1R
5 150073481 stop gained A/G;T snv 2
rs121913393
CSF1R
5 150054083 missense variant A/G snv 2
rs1801271
CSF1R
5 150054082 missense variant T/A;C snv 2
rs1057520014
CSF1R
5 150073480 missense variant C/A snv 1
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs121913506
KIT
0.677 0.320 4 54733154 missense variant G/A;C;T snv 24
rs5743551
TLR1
0.742 0.240 4 38806033 intron variant T/A;C snv 12
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 9
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs757333753
RAF1
0.851 0.200 3 12618681 missense variant C/A;T snv 4.0E-06 6
rs1800023
CCR5 ; CCR5AS
1.000 0.040 3 46370817 intron variant A/G snv 0.29 2