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: rs120074192
rs120074192
10 0.763 0.120 11 2527959 missense variant A/G snv 0.050 1.000 5 2003 2018
dbSNP: rs199472708
rs199472708
4 0.882 0.080 11 2572015 missense variant G/A snv 0.030 1.000 3 2014 2018
dbSNP: rs199472687
rs199472687
5 0.827 0.120 11 2527962 missense variant G/A snv 0.020 1.000 2 2008 2012
dbSNP: rs199472689
rs199472689
1 1.000 0.080 11 2527981 missense variant A/G snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs199472709
rs199472709
7 0.790 0.120 11 2572021 missense variant G/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs199473444
rs199473444
2 1.000 0.080 11 2445138 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs199473457
rs199473457
12 0.827 0.200 11 2572020 missense variant C/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs199956744
rs199956744
1 1.000 0.080 11 2572050 missense variant G/A;T snv 1.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs75813654
rs75813654
1 1.000 0.080 11 2571339 missense variant G/A;C;T snv 1.9E-04; 4.0E-06; 4.0E-06 0.010 1.000 1 2019 2019