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: rs121909208
rs121909208
13 0.724 0.240 5 136056780 missense variant C/T snv 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs762267106
rs762267106
GSN
1 1.000 0.080 9 121328963 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs121909215
rs121909215
7 0.790 0.200 5 136060898 missense variant G/A snv 0.720 1.000 2 2001 2010
dbSNP: rs121909210
rs121909210
15 0.708 0.200 5 136046406 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.030 1.000 3 1998 2010
dbSNP: rs121909209
rs121909209
9 0.763 0.160 5 136056781 missense variant G/A snv 0.040 1.000 4 1998 2012
dbSNP: rs121909211
rs121909211
15 0.724 0.200 5 136046407 missense variant G/A;T snv 4.0E-05 0.880 1.000 10 1998 2019