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: rs121909211
rs121909211
12 0.744 0.143 5 136046407 missense variant G/A,T snp 4.0E-05 0.860 1.000 12 1998 2013
dbSNP: rs121909215
rs121909215
6 0.801 0.143 5 136060898 missense variant G/A snp 0.720 1.000 3 2001 2010
dbSNP: rs121909209
rs121909209
5 0.821 0.071 5 136056781 missense variant G/A snp 0.020 1.000 2 1998 2007
dbSNP: rs121909208
rs121909208
7 0.801 0.071 5 136056780 missense variant C/T snp 0.010 1.000 1 2005 2005
dbSNP: rs121909210
rs121909210
11 0.734 0.143 5 136046406 missense variant C/A,T snp 4.0E-06; 4.0E-06 3.2E-05 0.010 1.000 1 1998 1998
dbSNP: rs762267106
rs762267106
GSN
1 1.000 0.071 9 121328963 missense variant A/G,T snp 4.0E-06; 4.0E-06 3.2E-05 0.010 1.000 1 2001 2001