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: rs2476491
rs2476491
IL2RA
8 0.776 0.240 10 6053447 intron variant A/T snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2284033
rs2284033
IL2RB
7 0.790 0.160 22 37137994 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs2266959
rs2266959
UBE2L3
9 0.776 0.200 22 21568615 intron variant G/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs1823549
rs1823549 		3 0.882 0.120 1 102682275 intergenic variant T/C snv 0.89 0.700 1.000 1 2017 2017
dbSNP: rs149850873
rs149850873
PTPN2
6 0.807 0.120 18 12885121 intron variant G/A snv 1.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs1479924
rs1479924 		6 0.807 0.120 4 122466445 intergenic variant G/A snv 0.76 0.700 1.000 1 2013 2013
dbSNP: rs1279094
rs1279094 		3 0.882 0.120 9 11706771 intron variant T/C snv 0.43 0.700 1.000 1 2017 2017
dbSNP: rs12517545
rs12517545
LINC01331
3 0.882 0.120 5 74384489 intron variant G/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs1178121
rs1178121
HDAC9
3 0.882 0.120 7 18723029 intron variant C/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs11714843
rs11714843
TIMMDC1
6 0.807 0.120 3 119502217 intron variant T/A snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs114940806
rs114940806
KLF17
3 0.882 0.120 1 44093000 intron variant A/G snv 5.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs11074967
rs11074967
RMI2 ; LOC400499 ; LOC105371082
6 0.807 0.120 16 11377557 intron variant C/G snv 0.36 0.700 1.000 1 2013 2013
dbSNP: rs10849448
rs10849448
LTBR
6 0.807 0.120 12 6384185 5 prime UTR variant A/G snv 0.82 0.700 1.000 1 2013 2013
dbSNP: rs10213692
rs10213692
ANKRD55
6 0.807 0.120 5 56146422 intron variant T/C snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs10194635
rs10194635
LINC01104
6 0.807 0.120 2 100217755 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10174238
rs10174238
STAT4
14 0.724 0.200 2 191108308 intron variant G/A snv 0.70 0.700 1.000 1 2013 2013