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: rs9532434
rs9532434
COG6
8 0.807 0.120 13 39781776 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs34132030
rs34132030
LINC02341
6 0.807 0.120 13 42481900 intron variant C/T snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs481331
rs481331 		3 0.882 0.120 10 42507600 intergenic variant A/T snv 0.80 0.700 1.000 1 2017 2017
dbSNP: rs72632736
rs72632736 		3 0.882 0.120 1 4389144 intergenic variant A/G snv 4.3E-02 0.700 1.000 1 2017 2017
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: rs79893749
rs79893749
CCR3
6 0.807 0.120 3 46212159 intron variant C/T snv 0.10 0.700 1.000 1 2013 2013
dbSNP: rs79575701
rs79575701
ZBTB7C
3 0.882 0.120 18 48053250 intron variant C/A;T snv 0.700 1.000 1 2017 2017
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: rs7909519
rs7909519
IL2RA
6 0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 0.700 1.000 1 2013 2013
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: 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: rs864089
rs864089
PRICKLE2
3 0.882 0.120 3 64258442 intron variant T/C snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs3825568
rs3825568
ZFP36L1
6 0.807 0.120 14 68793871 5 prime UTR variant C/G;T snv 0.700 1.000 1 2013 2013
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: rs7069750
rs7069750
FAS
6 0.807 0.120 10 89002619 non coding transcript exon variant G/C;T snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs27293
rs27293
LNPEP
6 0.807 0.120 5 97021474 intron variant A/G;T snv 0.700 1.000 1 2013 2013