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: rs10100465
rs10100465
LOC105375721
1 1.000 0.040 8 117614040 intergenic variant G/A snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs10114470
rs10114470
TNFSF15
4 0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs1040079
rs1040079
PACRG
3 0.882 0.040 6 162792995 intron variant A/G snv 0.31 0.020 1.000 2 2006 2012
dbSNP: rs10414149
rs10414149
SIGLEC5
1 1.000 0.040 19 51624491 intron variant A/G snv 0.30 0.700 1.000 1 2015 2015
dbSNP: rs1049432
rs1049432
TFAM
2 0.925 0.040 10 58395360 3 prime UTR variant G/C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs10507522
rs10507522
LOC107984576
1 1.000 0.040 13 43904864 intron variant A/G snv 0.11 0.710 1.000 2 2009 2016
dbSNP: rs1065489
rs1065489
CFH
19 0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 0.010 1.000 1 2013 2013
dbSNP: rs1071630
rs1071630
HLA-DQA1 ; HLA-DQA2 ; LOC107986589
4 0.851 0.120 6 32641349 missense variant T/A;C snv 0.49 0.010 1.000 1 2010 2010
dbSNP: rs10817758
rs10817758
DELEC1
1 1.000 0.040 9 115381654 intron variant C/T snv 0.13 0.700 1.000 1 2015 2015
dbSNP: rs10905284
rs10905284
GATA3
4 0.882 0.200 10 8073399 intron variant C/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10982385
rs10982385 		1 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 0.700 1.000 1 2009 2009
dbSNP: rs11003124
rs11003124
MBL2
2 1.000 0.040 10 52772131 upstream gene variant T/G snv 0.30 0.010 1.000 1 2013 2013
dbSNP: rs11174812
rs11174812
SLC2A13
1 1.000 0.040 12 40031285 intron variant C/T snv 0.36 0.700 1.000 1 2015 2015
dbSNP: rs11362
rs11362
DEFB1
13 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 0.010 1.000 1 2009 2009
dbSNP: rs121917864
rs121917864
TLR2
31 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 0.010 1.000 1 2005 2005
dbSNP: rs12631031
rs12631031
PARL
2 0.925 0.040 3 183857982 intron variant G/A snv 0.12 0.010 1.000 1 2016 2016
dbSNP: rs13220141
rs13220141 		1 1.000 0.040 6 146576497 intergenic variant A/T snv 8.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs1333955
rs1333955
PACRG
4 0.851 0.080 6 162792422 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs148704956
rs148704956
IL17A
19 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1554286
rs1554286
IL10 ; IL19
7 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 0.010 1.000 1 2011 2011
dbSNP: rs1587601
rs1587601 		1 1.000 0.040 5 35254508 intergenic variant A/G snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs160451
rs160451 		1 1.000 0.040 8 89650713 intron variant T/C snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs16948876
rs16948876 		1 1.000 0.040 16 50820507 intergenic variant G/A snv 6.2E-02 0.800 1.000 2 2011 2015
dbSNP: rs1799724
rs1799724
LTA ; TNF
47 0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 0.010 1.000 1 2015 2015