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: rs146597587
rs146597587
IL33 ; LOC107987046
1 1.000 0.080 9 6255967 splice acceptor variant G/C snv 2.2E-03 2.0E-03 0.720 1.000 3 2017 2019
dbSNP: rs1588265
rs1588265
PDE4D
1 1.000 0.080 5 60073967 intron variant A/G;T snv 0.800 1.000 3 2009 2011
dbSNP: rs2244012
rs2244012
RAD50
1 1.000 0.080 5 132565533 intron variant A/G snv 0.33 0.820 1.000 3 2010 2016
dbSNP: rs744910
rs744910
SMAD3
1 1.000 0.080 15 67154447 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs9840993
rs9840993
MYLK
1 1.000 0.080 3 123739046 missense variant G/A snv 0.95 0.88 0.030 1.000 3 2007 2015
dbSNP: rs1046295
rs1046295
PHF11 ; SETDB2-PHF11
1 1.000 0.080 13 49528674 3 prime UTR variant G/A snv 0.50 0.48 0.020 1.000 2 2010 2011
dbSNP: rs11778371
rs11778371
CHRNA2
1 1.000 0.080 8 27462388 intron variant C/T snv 4.0E-02 0.700 1.000 2 2009 2010
dbSNP: rs1544791
rs1544791
PDE4D
1 1.000 0.080 5 60143255 intron variant T/A;C snv 0.710 1.000 2 2009 2016
dbSNP: rs1810132
rs1810132
ERBB2
1 1.000 0.080 17 39709752 intron variant C/T snv 0.64 0.700 1.000 2 2010 2011
dbSNP: rs2236647
rs2236647
STIP1
1 1.000 0.080 11 64197133 non coding transcript exon variant C/T snv 0.53 0.020 1.000 2 2017 2019
dbSNP: rs2271308
rs2271308
STARD3
1 1.000 0.080 17 39661229 non coding transcript exon variant T/C snv 0.61 0.700 1.000 2 2010 2011
dbSNP: rs2548659
rs2548659
PDE4D
1 1.000 0.080 5 60088059 intron variant A/G snv 0.28 0.700 1.000 2 2009 2010
dbSNP: rs2941504
rs2941504
PGAP3
1 1.000 0.080 17 39674647 synonymous variant A/G snv 0.67 0.64 0.710 1.000 2 2010 2011
dbSNP: rs4378650
rs4378650
ORMDL3
1 1.000 0.080 17 39924612 intron variant A/G;T snv 0.020 1.000 2 2008 2009
dbSNP: rs4987053
rs4987053
CCR3
1 1.000 0.080 3 46265209 synonymous variant T/C snv 9.2E-02; 4.0E-06 9.1E-02 0.020 0.500 2 2001 2007
dbSNP: rs6591255
rs6591255
GSTP1
1 1.000 0.080 11 67582077 upstream gene variant T/A snv 0.38 0.020 1.000 2 2008 2009
dbSNP: rs7219080
rs7219080
GSDMA
1 1.000 0.080 17 39958263 intron variant A/C snv 0.65 0.710 1.000 2 2010 2016
dbSNP: rs936170
rs936170
MYLK ; LOC105369194
1 1.000 0.080 3 123703970 intron variant G/A;C snv 0.020 1.000 2 2007 2012
dbSNP: rs983280
rs983280
PDE4D
1 1.000 0.080 5 60149310 intron variant C/T snv 0.68 0.700 1.000 2 2009 2010
dbSNP: rs10021288
rs10021288 		1 1.000 0.080 4 122084379 downstream gene variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10048897
rs10048897
LINC00528
1 1.000 0.080 22 17777938 non coding transcript exon variant T/C snv 9.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs10056243
rs10056243 		1 1.000 0.080 5 110923378 intergenic variant G/A snv 8.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1007654
rs1007654
GSDMA
1 1.000 0.080 17 39955101 intron variant A/G snv 0.69 0.700 1.000 1 2010 2010
dbSNP: rs1012307
rs1012307
LINC01931 ; MMADHC-DT
1 1.000 0.080 2 149798707 intron variant A/C snv 4.9E-02 0.700 1.000 1 2014 2014
dbSNP: rs10131490
rs10131490
RAD51B
1 1.000 0.080 14 68276590 intron variant A/G;T snv 0.700 1.000 1 2019 2019