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: rs2155433
rs2155433 		2 11 118742212 intron variant G/A snv 0.24 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: rs231804
rs231804 		4 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs2327832
rs2327832 		10 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs26232
rs26232
MACIR
4 0.925 0.160 5 103261019 intron variant C/T snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs2736340
rs2736340 		22 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs2816316
rs2816316
LOC105371664
5 0.882 0.200 1 192567683 intron variant C/A snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs2893008
rs2893008
IL21-AS1
2 4 122631659 intron variant A/G snv 5.1E-02 0.700 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: rs3087243
rs3087243
CTLA4
44 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs3093023
rs3093023
CCR6 ; LOC105378122
7 0.851 0.160 6 167120802 intron variant G/A snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs3130544
rs3130544 		10 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs3184504
rs3184504
ATXN2 ; SH2B3
92 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.700 1.000 1 2011 2011
dbSNP: rs3748816
rs3748816
MMEL1
7 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 0.700 1.000 1 2011 2011
dbSNP: rs3761847
rs3761847
TRAF1
8 0.827 0.200 9 120927961 intron variant G/A snv 0.52 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: rs4288027
rs4288027
KIAA1109
2 4 122262050 intron variant A/C;G snv 0.13 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: rs4648356
rs4648356
TTC34
3 1.000 0.080 1 2792599 intron variant C/A snv 0.39 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: rs4750316
rs4750316
LINC02649 ; LINC02656
5 0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 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
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