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: rs4986790
rs4986790
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.090 0.778 9 2004 2015
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.070 0.857 7 2004 2015
dbSNP: rs1799962
rs1799962
IL9
3 0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02 0.010 1.000 1 2010 2010
dbSNP: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2013 2013
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
dbSNP: rs1800888
rs1800888
23 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2015 2015
dbSNP: rs2069885
rs2069885
IL9
5 0.851 0.120 5 135892476 missense variant G/A;C snv 0.11 0.010 1.000 1 2010 2010
dbSNP: rs3138557
rs3138557
4 0.851 0.080 12 68158711 intron variant CGAG/- delins 0.010 1.000 1 2014 2014
dbSNP: rs3732378
rs3732378
48 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006
dbSNP: rs4543123
rs4543123
4 0.882 0.080 4 38790903 non coding transcript exon variant A/G snv 0.32 0.010 1.000 1 2012 2012
dbSNP: rs4588
rs4588
GC
53 0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 0.010 1.000 1 2014 2014
dbSNP: rs7041
rs7041
GC
64 0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs757275190
rs757275190
1 1.000 9 131129441 missense variant T/A snv 0.010 1.000 1 2017 2017
dbSNP: rs909253
rs909253
34 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2009 2009