Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070901
FCER1G
0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 4
rs2746071
RGS2
0.882 0.160 1 192808434 intron variant A/G snv 0.35 4
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv 4
rs903361
ADORA1
0.882 0.160 1 203122146 intron variant G/A;C snv 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10917661
FCGR2B
0.882 0.160 1 161671427 stop gained C/T snv 2.8E-05 3
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs1214598
LOC101928512 ; CD247
0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs3001978
PUDPP2 ; RPTN
0.882 0.160 1 152153991 3 prime UTR variant T/C snv 0.50 3
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs369252
OBSCN
0.882 0.400 1 228344451 intron variant T/G snv 0.74 3
rs6692977
FCRL5
0.882 0.200 1 157517598 intron variant T/C;G snv 3
rs7518129
TNFSF4
0.882 0.120 1 173194429 intron variant A/G snv 0.47 3
rs7523907
LOC101928512 ; CD247
1.000 0.080 1 167458010 non coding transcript exon variant C/A;T snv 3
rs7534334
LELP1
0.882 0.160 1 153205376 downstream gene variant C/T snv 0.25 3
rs10158467 0.925 0.080 1 173162354 regulatory region variant A/G;T snv 2
rs10789340
LOC105378797
0.925 0.120 1 72474590 intron variant A/G;T snv 2
rs10924993 0.925 0.080 1 236296485 intergenic variant T/A;G snv 2
rs11102930
NGF-AS1 ; NGF
0.925 0.160 1 115338434 intron variant G/A snv 0.54 2
rs1188722
OBSCN
0.925 0.240 1 228276575 missense variant T/C snv 0.68 0.70 2
rs12023876
ADORA1
0.925 0.080 1 203124073 intron variant G/A;T snv 2
rs12122228
NFIA ; LOC105378764
0.925 0.160 1 60890848 intron variant G/A;T snv 2
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs12743520
EVI5
1.000 0.080 1 92571555 intron variant C/A snv 0.20 2