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: rs1016988
rs1016988 		4 5 132408882 upstream gene variant T/C snv 0.20 0.800 1.000 1 2009 2009
dbSNP: rs10226084
rs10226084 		3 7 17957989 upstream gene variant T/C snv 0.46 0.800 1.000 1 2013 2013
dbSNP: rs11242111
rs11242111
IRF1-AS1 ; LINC02863
3 5 132420366 intron variant A/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs1154988
rs1154988 		7 3 136206349 upstream gene variant T/A snv 0.76 0.800 1.000 1 2013 2013
dbSNP: rs12511469
rs12511469 		3 4 154530607 downstream gene variant T/A snv 0.18 0.800 1.000 1 2011 2011
dbSNP: rs12651106
rs12651106
DCHS2
3 4 154379907 intron variant C/A snv 0.12 0.800 1.000 1 2011 2011
dbSNP: rs12712127
rs12712127
IL1R1
3 2 102110201 intron variant A/G snv 0.62 0.800 1.000 1 2013 2013
dbSNP: rs12915708
rs12915708
SPPL2A
3 15 50756405 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs16844401
rs16844401
HGFAC
4 1.000 0.040 4 3447925 missense variant G/A;T snv 7.5E-02; 8.3E-06 0.800 1.000 1 2013 2013
dbSNP: rs1800788
rs1800788
FGB
3 4 154562762 upstream gene variant C/T snv 0.18 0.800 1.000 1 2011 2011
dbSNP: rs1938492
rs1938492 		3 1 65652146 intergenic variant A/C snv 0.43 0.800 1.000 1 2013 2013
dbSNP: rs2106854
rs2106854
IRF1-AS1
3 5 132433482 intron variant C/T snv 0.23 0.800 1.000 1 2013 2013
dbSNP: rs2286503
rs2286503
TOMM7
3 7 22816987 intron variant C/T snv 0.48 0.800 1.000 1 2013 2013
dbSNP: rs2522056
rs2522056
IRF1-AS1
4 5 132466034 intron variant G/A snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs434943
rs434943 		3 14 68847342 intergenic variant G/A snv 0.27 0.800 1.000 1 2013 2013
dbSNP: rs511154
rs511154 		3 3 136232079 intergenic variant A/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs6050
rs6050
FGA
10 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.800 1.000 1 2011 2011
dbSNP: rs7204230
rs7204230
CHD9
3 16 53158419 intron variant T/C snv 0.31 0.800 1.000 1 2013 2013
dbSNP: rs7681423
rs7681423 		5 4 154621096 intergenic variant C/T snv 0.26 0.800 1.000 1 2011 2011
dbSNP: rs7896783
rs7896783
JMJD1C
3 10 63402393 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs7968440
rs7968440
DIP2B
3 12 50740958 intron variant A/G snv 0.28 0.800 1.000 1 2013 2013
dbSNP: rs10034922
rs10034922 		3 4 154599476 downstream gene variant G/A snv 5.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs1012793
rs1012793
IRF1-AS1
1 5 132445653 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs1019670
rs1019670
MS4A6A
1 11 60173126 missense variant T/A snv 0.700 1.000 1 2013 2013
dbSNP: rs1029738
rs1029738
LOC112267993
1 7 22834428 downstream gene variant C/A snv 0.23 0.700 1.000 1 2017 2017