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: rs1047763
rs1047763
2 0.925 0.120 7 7243938 3 prime UTR variant G/A snv 0.22 0.010 1.000 1 2012 2012
dbSNP: rs373544789
rs373544789
2 0.925 0.120 19 54889688 missense variant G/A;T snv 8.8E-05; 3.2E-05 0.010 1.000 1 2007 2007
dbSNP: rs35366573
rs35366573
3 0.882 0.120 1 207785101 missense variant C/T snv 1.5E-02 1.5E-02 0.010 1.000 1 2008 2008
dbSNP: rs2239785
rs2239785
5 0.827 0.240 22 36265284 missense variant G/A snv 0.79 0.68 0.700 1.000 1 2010 2010
dbSNP: rs267602852
rs267602852
WT1
7 0.827 0.160 11 32417631 missense variant G/A snv 0.700 0
dbSNP: rs1222213359
rs1222213359
62 0.574 0.720 6 43770966 missense variant G/A snv 0.020 1.000 2 2011 2014
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2012 2012