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: rs1020388
rs1020388 		2 5 56264200 upstream gene variant T/G snv 0.34 0.800 1.000 1 2011 2011
dbSNP: rs11712165
rs11712165
ARHGAP31
5 0.882 0.200 3 119399949 intron variant T/G snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs2056626
rs2056626
CD247
5 0.882 0.080 1 167451188 intron variant T/G snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs2249937
rs2249937
LOC112267968
3 1.000 0.080 6 159094277 non coding transcript exon variant T/G snv 0.76 0.700 1.000 1 2011 2011
dbSNP: rs2280141
rs2280141
PLEKHA1
4 1.000 0.040 10 122433665 3 prime UTR variant T/G snv 0.56 0.700 1.000 1 2011 2011
dbSNP: rs6726160
rs6726160
NONOP2
3 1.000 0.080 2 60937594 non coding transcript exon variant T/G snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs7574865
rs7574865
STAT4
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.800 1.000 1 2011 2011
dbSNP: rs11981433
rs11981433
PON2
4 0.882 0.240 7 95425028 intron variant T/C;G snv 0.010 < 0.001 1 2011 2011
dbSNP: rs7579944
rs7579944 		5 0.882 0.200 2 30222160 intergenic variant T/C;G snv 0.800 1.000 1 2011 2011
dbSNP: rs10488631
rs10488631
TNPO3
13 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs11043097
rs11043097
LINC02752
2 11 11114248 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs1194849
rs1194849
SPRED2
2 2 65379519 intron variant T/C snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs13315591
rs13315591
FAM107A ; LOC107984079
4 0.925 0.160 3 58571114 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs1738074
rs1738074
TAGAP ; LOC105378083 ; LOC107986664
9 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs1953126
rs1953126
PHF19
3 1.000 0.120 9 120878222 intron variant T/C snv 0.68 0.800 1.000 1 2011 2011
dbSNP: rs296547
rs296547
MROH3P
5 0.882 0.200 1 200923009 intron variant T/C snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs3890745
rs3890745
MMEL1
4 0.925 0.200 1 2622185 intron variant T/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs4374642
rs4374642
KIAA1109
2 4 122179956 intron variant T/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs4626515
rs4626515 		2 7 140204330 intergenic variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs4675374
rs4675374
ICOS ; LOC101927840
5 0.882 0.200 2 203937855 intron variant T/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs4819388
rs4819388
ICOSLG
9 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 0.700 1.000 1 2011 2011
dbSNP: rs4958881
rs4958881
TNIP1
7 0.827 0.280 5 151070675 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs6933404
rs6933404 		5 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs9295089
rs9295089
TAGAP ; LOC105378083
2 6 159042932 non coding transcript exon variant T/C snv 0.20 0.700 1.000 1 2011 2011
dbSNP: rs4810485
rs4810485
CD40
16 0.732 0.480 20 46119308 intron variant T/A;G snv 0.700 1.000 1 2011 2011