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: rs121918093
rs121918093
TTR
3 0.882 0.200 18 31592944 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 1996 1996
dbSNP: rs121918098
rs121918098
TTR
5 0.807 0.200 18 31592939 missense variant A/G snv 0.010 1.000 1 2003 2003
dbSNP: rs28933979
rs28933979
TTR
68 0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 0.010 1.000 1 2004 2004