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: rs6441961
rs6441961
UQCRC2P1
1 1.000 0.080 3 46310893 non coding transcript exon variant T/C snv 0.74 0.810 1.000 3 2008 2015
dbSNP: rs11875687
rs11875687
PTPN2
1 1.000 0.080 18 12843138 intron variant T/C snv 0.17 0.800 1.000 2 2011 2012
dbSNP: rs182429
rs182429
LOC105378083 ; LOC107986664
1 1.000 0.080 6 159048542 intron variant A/G snv 0.49 0.800 1.000 2 2011 2012
dbSNP: rs2387397
rs2387397
LINC02649
1 1.000 0.080 10 6348230 intron variant G/A;C snv 0.800 1.000 2 2011 2012
dbSNP: rs4445406
rs4445406
MMEL1
1 1.000 0.080 1 2607961 intron variant T/C snv 0.41 0.800 1.000 2 2011 2012
dbSNP: rs6691768
rs6691768
NFIA
1 1.000 0.080 1 61326191 intron variant G/A;C snv 0.800 1.000 2 2010 2016
dbSNP: rs6715106
rs6715106
STAT4
1 1.000 0.080 2 191048308 intron variant A/G snv 6.1E-02 0.800 1.000 2 2011 2012
dbSNP: rs77027760
rs77027760 		1 1.000 0.080 6 137680924 intron variant G/A snv 0.15 0.700 1.000 2 2011 2012
dbSNP: rs7753008
rs7753008
BACH2
1 1.000 0.080 6 90099920 intron variant T/A;C snv 0.800 1.000 2 2011 2012
dbSNP: rs79758729
rs79758729
ELMO1
1 1.000 0.080 7 37378851 intron variant A/G snv 7.9E-02 0.700 1.000 2 2011 2012
dbSNP: rs1018326
rs1018326
LINC01934
1 1.000 0.080 2 181143073 intron variant T/C snv 0.47 0.800 1.000 1 2011 2011
dbSNP: rs1033180
rs1033180 		1 1.000 0.080 6 383546 regulatory region variant C/T snv 5.4E-02 0.800 1.000 1 2010 2010
dbSNP: rs10484718
rs10484718
THEMIS
1 1.000 0.080 6 127859906 intron variant A/T snv 8.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs10796045
rs10796045 		1 1.000 0.080 10 6360779 intergenic variant G/T snv 0.79 0.700 1.000 1 2014 2014
dbSNP: rs10800746
rs10800746
INAVA
1 1.000 0.080 1 200912264 intron variant C/T snv 0.32 0.800 1.000 1 2011 2011
dbSNP: rs10886159
rs10886159 		1 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 0.800 1.000 1 2013 2013
dbSNP: rs11100722
rs11100722 		1 1.000 0.080 4 141616307 intergenic variant G/C snv 0.77 0.010 1.000 1 2017 2017
dbSNP: rs11734090
rs11734090
KIAA1109
1 1.000 0.080 4 122306958 intron variant T/C snv 0.25 0.700 1.000 1 2014 2014
dbSNP: rs11851414
rs11851414
ZFP36L1
1 1.000 0.080 14 68792785 intron variant T/C snv 0.25 0.800 1.000 1 2011 2011
dbSNP: rs12142280
rs12142280 		1 1.000 0.080 1 172895512 intron variant T/A snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs1250557
rs1250557
ZMIZ1
1 1.000 0.080 10 79306017 intron variant G/T snv 0.63 0.700 1.000 1 2016 2016
dbSNP: rs12727642
rs12727642 		1 1.000 0.080 1 7986612 upstream gene variant C/A snv 0.12 0.800 1.000 1 2010 2010
dbSNP: rs13096142
rs13096142
CCR3
1 1.000 0.080 3 46240253 intron variant C/T snv 0.25 0.800 1.000 1 2014 2014
dbSNP: rs13401064
rs13401064
STAT4
1 1.000 0.080 2 191105604 intron variant C/G snv 8.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs1378938
rs1378938 		1 1.000 0.080 15 74804102 downstream gene variant T/A;C snv 0.800 1.000 1 2011 2011