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: rs73300638
rs73300638
JAZF1
6 0.807 0.120 7 28147725 intron variant A/C;G snv 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 0.700 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: 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: 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: rs9532434
rs9532434
COG6
8 0.807 0.120 13 39781776 intron variant T/A;C snv 0.700 1.000 1 2013 2013