Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 7
rs3132468
MICB
0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
rs1131691564
NR0B1
0.925 0.160 X 30308656 stop gained C/T snv 2
rs1324519932
NR0B1
0.925 0.160 X 30308445 stop gained C/A;G snv 1.3E-05 9.5E-06 2
rs1555973010
NR0B1
0.925 0.160 X 30308463 stop gained G/A snv 2
rs1555973115
NR0B1
0.925 0.160 X 30308812 frameshift variant TT/-;T delins 2
rs1555973131
NR0B1
0.925 0.160 X 30308848 stop gained C/T snv 2
rs767828388
NR0B1
0.925 0.160 X 30308836 stop gained G/A;C snv 6.1E-06 2