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: rs13003464
rs13003464
PUS10
7 0.827 0.200 2 60959694 intron variant A/G snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs13010713
rs13010713
LINC01934
5 0.882 0.200 2 181131318 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs13031237
rs13031237
REL
3 1.000 0.120 2 60908994 intron variant G/T snv 0.25 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: rs13119723
rs13119723
KIAA1109
8 0.807 0.280 4 122297158 intron variant A/G snv 0.10 0.700 1.000 1 2011 2011
dbSNP: rs13151961
rs13151961
KIAA1109
7 0.827 0.200 4 122194347 intron variant A/G snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs13314993
rs13314993
LOC105377022
5 0.882 0.200 3 32973977 regulatory region variant G/C;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: rs1355208
rs1355208 		2 2 30222456 intergenic variant A/G snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs1464510
rs1464510
LPP
9 0.807 0.280 3 188394766 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1678542
rs1678542
KIF5A
9 0.790 0.320 12 57574932 intron variant C/G snv 0.42 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: rs17035378
rs17035378
PLEK ; LOC101927723
5 0.882 0.200 2 68371823 intron variant T/A;C snv 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: rs1772408
rs1772408
IFI16
2 1 159035859 intron variant A/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546
IL12A-AS1
7 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 0.700 1.000 1 2011 2011
dbSNP: rs17876183
rs17876183
PON2
1 7 95434956 missense variant C/T snv 1.2E-02 1.4E-02 0.010 < 0.001 1 2011 2011
dbSNP: rs17876205
rs17876205 		1 7 95403792 downstream gene variant C/G snv 1.4E-02 0.010 < 0.001 1 2011 2011
dbSNP: rs1876518
rs1876518
SPRED2
2 2 65381775 intron variant C/T snv 0.45 0.800 1.000 1 2011 2011
dbSNP: rs1893217
rs1893217
PTPN2
14 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.800 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: 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: rs212388
rs212388
LOC105378083 ; LOC112267968
8 0.827 0.240 6 159069404 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs212389
rs212389
LOC105378083 ; LOC112267968
4 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs212402
rs212402
LOC105378083
3 1.000 0.080 6 159051263 intron variant G/A snv 0.66 0.700 1.000 1 2011 2011