Source: ALL
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: rs121909715
rs121909715
GSN
8 0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 0.040 1.000 4 1995 2011
dbSNP: rs759304648
rs759304648
GSN
9 0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 0.040 1.000 4 1995 2000
dbSNP: rs920832709
rs920832709
GSN
4 0.851 0.200 9 121321384 synonymous variant G/T snv 0.020 1.000 2 1995 2000
dbSNP: rs750132751
rs750132751
GSN
1 1.000 0.120 9 121310759 missense variant G/A snv 3.2E-05 5.6E-05 0.010 1.000 1 2019 2019