Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs11264799
FCRL3
0.851 0.240 1 157700967 upstream gene variant C/T snv 0.28 6
rs7522061
FCRL3
0.882 0.320 1 157698600 missense variant T/C;G snv 0.45 0.51 4
rs1001703993
PPOX
0.882 0.120 1 161170696 missense variant G/A;T snv 8.0E-06 1.4E-05 3
rs11102930
NGF-AS1 ; NGF
0.925 0.160 1 115338434 intron variant G/A snv 0.54 2
rs11264794
FCRL3
1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 2
rs3795299
IL22RA1
0.925 0.200 1 24120978 missense variant G/A;C;T snv 9.6E-05; 0.42; 4.0E-06 2
rs11264793
FCRL3
1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28 1
rs12022418
LOC105371664
1.000 0.120 1 192565977 intron variant C/A snv 0.64 1
rs17019602
VAV3
1.000 0.120 1 107646236 intron variant A/G snv 0.19 1
rs6691569
FCRL3
1.000 0.120 1 157678308 3 prime UTR variant G/A snv 0.24 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs3218896
IL1R2
0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs3218977
IL1R2
0.807 0.240 2 102024739 3 prime UTR variant A/G snv 0.14 6
rs10490571
IL1R1
0.827 0.320 2 102100877 intron variant C/T snv 0.29 5
rs719250
IL1R2
0.827 0.200 2 102007256 intron variant C/T snv 0.11 5