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
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs1760944
OSGEP ; APEX1
0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs2230199
C3
0.763 0.240 19 6718376 missense variant G/C;T snv 0.15 10
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs61750172
GUCY2D
0.807 0.080 17 8014700 missense variant C/A;T snv 4.0E-06 8
rs179247
TSHR
0.882 0.160 14 80966202 intron variant A/G snv 0.40 5
rs201654095
CACNA1F
0.882 0.160 X 49224864 missense variant C/G snv 4
rs9463772
IL17F
0.925 0.240 6 52246993 non coding transcript exon variant C/A;T snv 3
rs17593222
STAT3
0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 3
rs11567847
TEAD1
0.925 0.120 11 12937202 missense variant T/C snv 3
rs3766404
CFH
1.000 0.040 1 196682702 intron variant T/C snv 0.22 2