Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs10774671
OAS1
0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs179008
TLR7
0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs1818879 0.827 0.120 7 22733108 downstream gene variant G/A;C snv 7
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins 5
rs4273729 0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv 5
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs179363879
AIRE
0.925 0.160 21 44286092 missense variant T/C snv 3
rs3136558
IL1B
1.000 2 112833698 intron variant A/G snv 0.21 4
rs12487066
LOC105374027
1.000 0.080 3 106193283 intron variant T/C snv 0.28 2
rs1480480967
IFNA13
1.000 0.080 9 21367884 missense variant C/T snv 4.0E-06 2
rs17886084
MMP1 ; WTAPP1
1.000 0.080 11 102799765 intron variant C/- delins 2
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06 2
rs781522558
STAT2
1.000 12 56346844 stop gained G/C;T snv 4.0E-06 2