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: rs6680578
rs6680578
EVI5
1 1.000 0.080 1 92711321 intron variant T/A snv 0.57 0.020 1.000 2 2010 2017
dbSNP: rs669607
rs669607
LINC01967
1 1.000 0.080 3 28029953 intron variant A/C snv 0.38 0.800 1.000 2 2011 2016
dbSNP: rs6896969
rs6896969 		1 1.000 0.080 5 40424324 intron variant A/C;G snv 0.57 0.800 1.000 2 2009 2011
dbSNP: rs756699
rs756699 		1 1.000 0.080 5 134110884 upstream gene variant C/T snv 0.80 0.800 1.000 2 2011 2013
dbSNP: rs7595037
rs7595037 		1 1.000 0.080 2 68419963 regulatory region variant C/T snv 0.57 0.800 1.000 2 2011 2019
dbSNP: rs8042861
rs8042861
IQGAP1
1 1.000 0.080 15 90434101 intron variant G/A;T snv 0.710 1.000 2 2013 2016
dbSNP: rs9828519
rs9828519
SLC9A9
1 1.000 0.080 3 143707136 intron variant G/A;C;T snv 0.020 1.000 2 2015 2017
dbSNP: rs1014486
rs1014486
IL12A-AS1
1 1.000 0.080 3 159973324 intron variant T/C snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs1044165
rs1044165
VSIG4
1 1.000 0.080 X 66021884 3 prime UTR variant G/A snv 9.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs10466829
rs10466829
CLECL1
1 1.000 0.080 12 9723495 intron variant G/A snv 0.55 0.800 1.000 1 2011 2011
dbSNP: rs10492503
rs10492503
GPC5
1 1.000 0.080 13 92232844 intron variant T/A snv 0.36 0.010 1.000 1 2019 2019
dbSNP: rs10500817
rs10500817
LOC102724957
1 1.000 0.080 11 15626589 intron variant T/C snv 0.12 0.700 1.000 1 2007 2007
dbSNP: rs1050391
rs1050391
HLA-DMA ; HLA-DMB
1 1.000 0.080 6 32950080 non coding transcript exon variant A/G snv 0.93 0.700 1.000 1 2007 2007
dbSNP: rs1059174
rs1059174
HLA-F ; HLA-F-AS1
1 1.000 0.080 6 29726650 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2007 2007
dbSNP: rs10823051
rs10823051
CTNNA3
1 1.000 0.080 10 67504839 intron variant G/C snv 0.13 0.700 1.000 1 2007 2007
dbSNP: rs10866713
rs10866713 		1 1.000 0.080 5 159491886 intron variant G/A snv 0.16 0.800 1.000 1 2011 2011
dbSNP: rs10877013
rs10877013
METTL1 ; EEF1AKMT3
1 1.000 0.080 12 57771302 intron variant C/T snv 0.38 0.32 0.010 1.000 1 2016 2016
dbSNP: rs10984447
rs10984447
BRINP1
1 1.000 0.080 9 119222275 intron variant A/G snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs11052877
rs11052877
CD69
1 1.000 0.080 12 9753094 3 prime UTR variant A/G snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs11086996
rs11086996 		1 1.000 0.080 20 46095024 upstream gene variant C/T snv 0.20 0.010 1.000 1 2013 2013
dbSNP: rs1109670
rs1109670
LOC105373414 ; LOC105373416
1 1.000 0.080 2 9109909 upstream gene variant C/A;G snv 0.010 1.000 1 2011 2011
dbSNP: rs11256593
rs11256593 		1 1.000 0.080 10 6075359 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
dbSNP: rs112852289
rs112852289
CD6 ; LOC105369326
1 1.000 0.080 11 61008833 frameshift variant -/T ins 5.1E-06; 5.1E-06 0.010 1.000 1 2013 2013
dbSNP: rs112913018
rs112913018
MOG
1 1.000 0.080 6 29670324 missense variant T/A;C snv 5.7E-04; 2.8E-03 0.010 1.000 1 2002 2002
dbSNP: rs113116201
rs113116201
MIR181A1HG
1 1.000 0.080 1 198861813 intron variant T/C snv 1.2E-02 0.700 1.000 1 2013 2013