Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs74597329
rs74597329
IFNL4
1 1.000 0.080 19 39248515 missense variant T/A;G snv 0.22 0.700 1.000 2 2019 2019
dbSNP: rs1013151
rs1013151
TLR8 ; TLR8-AS1
1 1.000 0.080 X 12914412 intron variant C/T snv 0.51 0.010 1.000 1 2015 2015
dbSNP: rs1029153
rs1029153
CXCL12
1 1.000 0.080 10 44371698 3 prime UTR variant A/G snv 0.27 0.010 1.000 1 2016 2016
dbSNP: rs1034713634
rs1034713634
VIPR1
1 1.000 0.080 3 42536097 missense variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1049807
rs1049807
CCL4 ; LOC101927369
1 1.000 0.080 17 36105270 missense variant A/G snv 0.22 0.21 0.010 1.000 1 2018 2018
dbSNP: rs1052020291
rs1052020291
CTSB
1 1.000 0.080 8 11848075 missense variant G/C snv 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1063340
rs1063340
CCL3 ; LOC102724850
1 1.000 0.080 17 36088417 3 prime UTR variant G/C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs1063478
rs1063478
HLA-DMA ; HLA-DMB
1 1.000 0.080 6 32949767 missense variant C/T snv 0.15 0.13 0.010 1.000 1 2014 2014
dbSNP: rs111511318
rs111511318 		1 1.000 0.080 5 156998817 intergenic variant C/A snv 2.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs11249006
rs11249006
IFNLR1
1 1.000 0.080 1 24155984 3 prime UTR variant G/A snv 0.30 0.010 1.000 1 2011 2011
dbSNP: rs1156458285
rs1156458285
IFNA1
1 1.000 0.080 9 21440717 missense variant G/C snv 0.010 1.000 1 2015 2015
dbSNP: rs116399066
rs116399066 		1 1.000 0.080 1 143723149 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1178326401
rs1178326401
F2
1 1.000 0.080 11 46728826 synonymous variant G/A snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs1236515917
rs1236515917
IFNA13
1 1.000 0.080 9 21367798 missense variant C/G snv 4.4E-06 0.010 1.000 1 2015 2015
dbSNP: rs1303234079
rs1303234079
GSTK1 ; LOC105375545
1 1.000 0.080 7 143267656 missense variant G/A snv 8.0E-06 1.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs13401937
rs13401937
RTN4
1 1.000 0.080 2 55025078 splice region variant T/G snv 0.11 0.14 0.700 1.000 1 2019 2019
dbSNP: rs1484994
rs1484994
BCL2L1
1 1.000 0.080 20 31718172 intron variant A/G snv 0.38 0.010 1.000 1 2015 2015
dbSNP: rs1754257
rs1754257
GPR158
1 1.000 0.080 10 25385685 intron variant G/A snv 0.71 0.700 1.000 1 2019 2019
dbSNP: rs179012
rs179012
TLR7
1 1.000 0.080 X 12883443 intron variant G/A snv 0.42 0.010 1.000 1 2014 2014
dbSNP: rs179016
rs179016
TLR7
1 1.000 0.080 X 12876323 intron variant G/A;C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1800803
rs1800803
MTTP
1 1.000 0.080 4 99574424 intron variant A/T snv 0.43 0.010 1.000 1 2011 2011
dbSNP: rs1979860
rs1979860 		1 1.000 0.080 5 174586529 regulatory region variant C/T snv 1.8E-02 0.010 1.000 1 2013 2013
dbSNP: rs1997060
rs1997060
NLGN1
1 1.000 0.080 3 174035108 intron variant A/G snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs200664537
rs200664537
CTSB
1 1.000 0.080 8 11847084 missense variant G/A;C snv 4.0E-06; 1.2E-04 0.010 1.000 1 2019 2019
dbSNP: rs201065145
rs201065145
GPT ; LOC101928953
1 1.000 0.080 8 144505096 missense variant G/A snv 1.4E-04 3.5E-05 0.010 1.000 1 2016 2016