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: rs3024877
rs3024877
STAT4
1 1.000 0.120 2 191040163 intron variant C/T snv 0.35 0.010 1.000 1 2011 2011
dbSNP: rs3024908
rs3024908
STAT4 ; LOC105373805
1 1.000 0.120 2 191029415 intron variant T/C snv 9.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs3024912
rs3024912
LOC105373805
2 0.925 0.120 2 191028361 intron variant A/C snv 0.29 0.010 1.000 1 2011 2011
dbSNP: rs352139
rs352139
TLR9
18 0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 0.010 1.000 1 2013 2013
dbSNP: rs352140
rs352140
TLR9
42 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 0.010 1.000 1 2013 2013
dbSNP: rs35771982
rs35771982
PLA2R1
2 0.925 0.120 2 160028907 missense variant G/C snv 0.39 0.35 0.010 1.000 1 2014 2014
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2011 2011
dbSNP: rs4326755
rs4326755
TRPC6
1 1.000 0.120 11 101578627 intron variant G/A snv 0.48 0.010 < 0.001 1 2010 2010