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: 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: rs4664308
rs4664308
PLA2R1 ; LOC105373717
4 0.851 0.160 2 160060986 intron variant A/G snv 0.30 0.800 1.000 1 2011 2011
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: 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: rs17830558
rs17830558
PLA2R1
1 1.000 0.120 2 160021853 intron variant T/G snv 0.39 0.710 1.000 1 2017 2017
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
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: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2008 2008