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: 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: 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: rs6946509
rs6946509 		6 0.807 0.120 7 22769871 downstream gene variant T/A;C snv 0.700 1.000 1 2013 2013
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: rs10194635
rs10194635
LINC01104
6 0.807 0.120 2 100217755 intron variant T/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs8129030
rs8129030
RUNX1
7 0.807 0.120 21 35340290 intron variant T/A;G snv 0.72 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: rs45539732
rs45539732
STAT1
6 0.807 0.120 2 191009521 intron variant T/C snv 1.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs7775055
rs7775055 		7 0.790 0.200 6 32690139 TF binding site variant T/C snv 6.2E-02 0.800 1.000 1 2013 2013
dbSNP: rs7909519
rs7909519
IL2RA
6 0.807 0.120 10 6047878 intron variant T/G snv 7.2E-02 0.800 1.000 1 2013 2013