Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs200215055
FCGR3B
0.742 0.400 1 161626196 missense variant C/A;G;T snv 1.5E-03; 1.2E-05; 4.0E-06 11
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs1518111
IL19 ; IL10
0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs1308699981
FCGR3A
0.807 0.440 1 161543085 missense variant G/A snv 4.0E-06 7
rs2067079
GAS5 ; SNORA103 ; SNORD80 ; SNORD77 ; SNORD81 ; SNORD44 ; SNORD78 ; SNORD47 ; SNORD79
0.807 0.240 1 173866073 non coding transcript exon variant C/T snv 0.22 0.18 7
rs3024498
IL10
0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs844648
TNFSF4 ; LOC100506023
0.807 0.280 1 173254724 regulatory region variant G/A snv 0.46 6
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs10489265
TNFSF4 ; LOC100506023
0.827 0.200 1 173266926 regulatory region variant A/C snv 0.21 5
rs12938
C1orf112 ; SELL
0.851 0.160 1 169691640 3 prime UTR variant A/G snv 0.27 5
rs1518110
IL10 ; IL19
0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs17615
CR2
0.827 0.200 1 207473117 missense variant G/A snv 0.26 0.31 5
rs17849502
NCF2 ; SMG7
0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5