Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1805034
TNFRSF11A
0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 12
rs751093906
SLC20A2
0.882 0.200 8 42472255 stop gained G/A;C snv 4.0E-06 8
rs118204456
GRK6 ; F12 ; SLC34A1
0.851 0.200 5 177404231 missense variant G/C;T snv 4.3E-06 7
rs147080557
NLRP12
0.882 0.120 19 53810777 missense variant G/A;C snv 3.6E-05; 4.0E-06 6
rs12746200
PLA2G4A
0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02 6
rs1187636039
EPHA3
0.925 0.120 3 89341043 missense variant C/A snv 5
rs35211496
TNFRSF11A
0.851 0.200 18 62354528 missense variant C/T snv 0.12 0.12 5
rs9833094
ABI3BP
1.000 0.080 3 100872081 intron variant C/A;T snv 2
rs9323624
IFT43
1.000 0.080 14 76033960 intron variant T/C snv 0.50 2
rs2228246
PLCG1
0.925 0.120 20 41163423 missense variant A/G snv 0.14 0.14 2