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: rs10036748
rs10036748
TNIP1
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2012 2012
dbSNP: rs10168266
rs10168266
STAT4
8 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs10178332
rs10178332
ROCK2
2 0.925 0.120 2 11268891 intron variant C/A;G snv 0.010 1.000 1 2016 2016
dbSNP: rs10406069
rs10406069
CD22 ; MIR5196
1 1.000 0.040 19 35345627 missense variant G/A;C snv 0.16 0.010 1.000 1 2012 2012
dbSNP: rs10413500
rs10413500
CD22 ; MIR5196
1 1.000 0.040 19 35345923 intron variant C/G snv 0.16 0.010 1.000 1 2012 2012
dbSNP: rs10419538
rs10419538
CD22
1 1.000 0.040 19 35333116 intron variant C/G snv 0.11 0.010 1.000 1 2012 2012
dbSNP: rs10499194
rs10499194 		10 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 < 0.001 1 2010 2010
dbSNP: rs10744676
rs10744676
KCNA5
2 0.925 0.080 12 5043783 upstream gene variant C/T snv 0.88 0.010 1.000 1 2010 2010
dbSNP: rs10865710
rs10865710
PPARG
13 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs10912580
rs10912580
TNFSF4 ; LOC100506023
3 0.882 0.080 1 173287411 intergenic variant A/G snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs10946216
rs10946216
CCR6
1 1.000 0.040 6 167125409 intron variant T/C snv 0.61 0.010 1.000 1 2013 2013
dbSNP: rs10954213
rs10954213
IRF5
11 0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 0.010 1.000 1 2010 2010
dbSNP: rs11102522
rs11102522
RHOC
1 1.000 0.040 1 112708266 intron variant T/C snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs11117432
rs11117432 		4 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 0.010 1.000 1 2015 2015
dbSNP: rs11191865
rs11191865
STN1
3 0.925 0.160 10 103913084 intron variant G/A snv 0.44 0.010 1.000 1 2016 2016
dbSNP: rs11209026
rs11209026
IL23R
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs1130866
rs1130866
SFTPB
9 0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 0.010 1.000 1 2008 2008
dbSNP: rs1131665
rs1131665
IRF7
4 0.851 0.160 11 613208 missense variant T/C snv 0.25 0.33 0.010 1.000 1 2012 2012
dbSNP: rs1143634
rs1143634
IL1B
52 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 0.010 1.000 1 2015 2015
dbSNP: rs1143679
rs1143679
ITGAM
14 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 0.010 1.000 1 2012 2012
dbSNP: rs11465804
rs11465804
IL23R
10 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2009 2009
dbSNP: rs11538960
rs11538960
RHOC ; MOV10
1 1.000 0.040 1 112701565 missense variant C/T snv 4.2E-04 5.2E-04 0.010 1.000 1 2016 2016
dbSNP: rs11594656
rs11594656 		9 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 0.010 < 0.001 1 2012 2012
dbSNP: rs117026326
rs117026326
GTF2I ; LOC101926943
10 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2016 2016
dbSNP: rs1177506410
rs1177506410
AGT
12 0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2002 2002