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: rs951005
rs951005 		10 0.807 0.200 9 34743684 intron variant G/A snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs975730
rs975730 		2 8 128303768 intergenic variant G/A snv 0.45 0.800 1.000 1 2011 2011
dbSNP: rs9792269
rs9792269 		5 0.882 0.200 8 128252343 intergenic variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs11676922
rs11676922
AFF3
4 0.925 0.160 2 100190478 intron variant T/A snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs6859219
rs6859219
ANKRD55
4 0.925 0.160 5 56142753 intron variant C/A snv 0.20 0.700 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: rs548234
rs548234
ATG5
11 0.763 0.360 6 106120159 intron variant C/T snv 0.76 0.700 1.000 1 2011 2011
dbSNP: rs653178
rs653178
ATXN2
41 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.800 1.000 1 2011 2011
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: rs10806425
rs10806425
BACH2
6 0.851 0.280 6 90216893 intron variant C/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs13098911
rs13098911
CCR3
5 0.882 0.200 3 46193709 intron variant C/G;T snv 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: 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: rs864537
rs864537
CD247
4 0.925 0.200 1 167442147 intron variant A/G snv 0.29 0.800 1.000 1 2011 2011
dbSNP: rs7523907
rs7523907
CD247 ; LOC101928512
3 1.000 0.080 1 167458010 non coding transcript exon variant C/A;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: 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: rs756207760
rs756207760
CXCR4
2 2 136115275 missense variant C/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 1999 1999
dbSNP: rs10892286
rs10892286
DDX6
2 11 118771376 intron variant A/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs11984075
rs11984075
ELMO1
2 7 37397251 intron variant A/G snv 0.14 0.800 1.000 1 2011 2011
dbSNP: rs11221332
rs11221332
ETS1
13 0.763 0.280 11 128511079 intron variant C/A;T snv 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: rs17026688
rs17026688
GADL1
2 1.000 0.040 3 30845325 intron variant C/T snv 9.3E-03 0.010 1.000 1 2019 2019
dbSNP: rs2292832
rs2292832
GPC1 ; MIR149 ; LOC100130449
46 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 0.010 1.000 1 2019 2019
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