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: rs3088362
rs3088362
CCDC122
1 1.000 0.040 13 43859494 intron variant C/A;T snv 0.710 1.000 3 2009 2016
dbSNP: rs9356058
rs9356058
PACRG
1 1.000 0.040 6 162730367 intron variant C/A;T snv 0.020 1.000 2 2012 2013
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: 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: 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: rs10905284
rs10905284
GATA3
4 0.882 0.200 10 8073399 intron variant C/A;T snv 0.010 1.000 1 2016 2016
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: 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: rs1800972
rs1800972
DEFB1
16 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 0.010 1.000 1 2009 2009
dbSNP: rs2024825
rs2024825
C1orf141
1 1.000 0.040 1 67132294 intron variant T/A;C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs2221593
rs2221593
BATF3
1 1.000 0.040 1 212700089 upstream gene variant C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs2228570
rs2228570
VDR
99 0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 0.010 1.000 1 2019 2019
dbSNP: rs2270368
rs2270368
SNX20
2 0.925 0.080 16 50680424 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs2524132
rs2524132
HLA-B ; LINC02571 ; LOC112267902
1 1.000 0.040 6 31297135 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2844573
rs2844573 		3 0.882 0.160 6 31367677 intron variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs34411505
rs34411505 		1 1.000 0.040 16 27395368 intergenic variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs3753395
rs3753395
CFH
5 0.882 0.120 1 196717522 intron variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs4720118
rs4720118
BBS9
1 1.000 0.040 7 33429629 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs55894533
rs55894533 		1 1.000 0.040 8 11891733 downstream gene variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs58744688
rs58744688
FMNL1
1 1.000 0.040 17 45230816 intron variant A/C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs6863015
rs6863015 		1 1.000 0.040 5 159416227 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs7096206
rs7096206
MBL2
17 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs7298930
rs7298930
LRRK2
2 0.925 0.040 12 40325698 intron variant A/C;G;T snv 0.010 1.000 1 2015 2015