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: rs15895
rs15895
OAS2
1 1.000 0.040 12 113010483 stop lost A/G;T snv 0.75 0.010 < 0.001 1 2013 2013
dbSNP: rs4859584
rs4859584
ART3 ; CXCL10
1 1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 0.010 1.000 1 2015 2015
dbSNP: rs1285933
rs1285933
MGAM ; CLEC5A
2 0.925 0.040 7 141927349 intron variant G/A snv 0.54 0.010 1.000 1 2017 2017
dbSNP: rs1447043692
rs1447043692
HPSE2
2 0.925 0.040 10 98641918 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs3205166
rs3205166
DDX58
2 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 0.010 1.000 1 2015 2015
dbSNP: rs371057322
rs371057322
KIDINS220
2 0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 0.010 1.000 1 2007 2007
dbSNP: rs3739319
rs3739319
IDO1
2 0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 0.010 1.000 1 2019 2019
dbSNP: rs1131454
rs1131454
OAS1
3 0.882 0.040 12 112911065 missense variant G/A;C snv 0.57 0.010 < 0.001 1 2013 2013
dbSNP: rs1805016
rs1805016
IL4R
3 0.882 0.080 16 27363606 missense variant T/G snv 6.4E-02 0.13 0.010 1.000 1 2019 2019
dbSNP: rs5745568
rs5745568
BAK1 ; GGNBP1
4 0.882 0.080 6 33580617 intron variant G/T snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs6141
rs6141
THPO
4 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 0.010 1.000 1 2016 2016
dbSNP: rs669260
rs669260
DDX58
4 0.851 0.080 9 32503442 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs750898115
rs750898115
USO1
4 0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 0.010 1.000 1 2007 2007
dbSNP: rs1732778
rs1732778 		5 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 0.020 0.500 2 2013 2015
dbSNP: rs3132468
rs3132468
MICB
5 0.827 0.240 6 31507709 intron variant C/T snv 0.77 0.020 0.500 2 2013 2014
dbSNP: rs2285932
rs2285932
OAS3
5 0.851 0.120 12 112949145 synonymous variant T/C snv 0.76 0.78 0.010 < 0.001 1 2013 2013
dbSNP: rs735239
rs735239
CD209
5 0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs2072136
rs2072136
OAS3
6 0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 0.020 < 0.001 2 2013 2015
dbSNP: rs6065
rs6065
CHRNE ; GP1BA
6 0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 0.010 1.000 1 2016 2016
dbSNP: rs3740360
rs3740360
PLCE1
7 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 0.010 < 0.001 1 2013 2013
dbSNP: rs2287886
rs2287886
CD209
9 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 0.010 1.000 1 2013 2013
dbSNP: rs385893
rs385893 		9 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.010 1.000 1 2016 2016
dbSNP: rs739496
rs739496
ATXN2 ; SH2B3
10 0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 0.010 1.000 1 2016 2016
dbSNP: rs10774671
rs10774671
OAS1
14 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 0.010 < 0.001 1 2013 2013
dbSNP: rs4804803
rs4804803
CD209
15 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 0.070 1.000 7 2010 2018