Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3136558
rs3136558
IL1B
1.000 2 112833698 intron variant A/G snv 0.21
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2015 2015
dbSNP: rs3775291
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2012 2012
dbSNP: rs3789679
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs397516808
rs397516808
PTPN11
12 112446327 synonymous variant A/G snv 1.6E-05 1.4E-05
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2015 2015
dbSNP: rs4273729
rs4273729 		0.851 0.240 6 32710820 upstream gene variant C/A;G;T snv
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2017 2017
dbSNP: rs4553808
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs486907
rs486907
RNASEL
0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2006 2006
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2011 2011
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2011 2011
dbSNP: rs7269320
rs7269320
MAVS
20 3865750 missense variant C/T snv 0.16 0.21
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2019 2019
dbSNP: rs738409
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2012 2012
dbSNP: rs755850200
rs755850200
VDR
1.000 0.040 12 47846347 missense variant T/C snv 2.1E-05 7.0E-06
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2018 2018
dbSNP: rs781522558
rs781522558
STAT2
1.000 12 56346844 stop gained G/C;T snv 4.0E-06
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2015 2015
dbSNP: rs8099917
rs8099917 		0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs17886084
rs17886084
MMP1 ; WTAPP1
1.000 0.080 11 102799765 intron variant C/- delins
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs35068180
rs35068180
MMP3
0.851 0.040 11 102845217 upstream gene variant A/-;AA delins
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2013 2013
dbSNP: rs371194629
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		0.010 1.000 1 2016 2016