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: rs11551437
rs11551437
3 1.000 0.080 2 47161833 missense variant G/A snv 0.010 1.000 1 2016 2016
dbSNP: rs398124647
rs398124647
6 0.807 0.120 2 47161851 missense variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs398124648
rs398124648
2 0.925 0.080 2 47161748 missense variant A/C snv 0.010 1.000 1 2014 2014
dbSNP: rs398124649
rs398124649
2 0.925 0.080 2 47161737 missense variant T/G snv 0.010 1.000 1 2014 2014
dbSNP: rs398124650
rs398124650
3 0.882 0.120 2 47161744 missense variant C/G;T snv 0.010 1.000 1 2014 2014