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: rs28933979
rs28933979
TTR
68 0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 0.100 1.000 10 1985 2018
dbSNP: rs121918075
rs121918075
TTR
15 0.752 0.280 18 31598632 missense variant A/G snv 0.010 1.000 1 2005 2005
dbSNP: rs121918077
rs121918077
TTR
2 0.882 0.120 18 31592992 missense variant G/C snv 0.010 1.000 1 2018 2018
dbSNP: rs121918095
rs121918095
TTR
6 0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 0.010 1.000 1 2000 2000
dbSNP: rs121918098
rs121918098
TTR
5 0.807 0.200 18 31592939 missense variant A/G snv 0.010 1.000 1 2004 2004
dbSNP: rs138065384
rs138065384
TTR
3 0.925 0.040 18 31593016 missense variant T/C snv 4.4E-05 1.9E-04 0.010 1.000 1 2013 2013
dbSNP: rs76992529
rs76992529
TTR
29 0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 0.010 1.000 1 2001 2001