Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28933979
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.900 0.989 47 1984 2019
dbSNP: rs267607161
rs267607161
TTR
0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.870 1.000 7 1986 2020
dbSNP: rs76992529
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.860 1.000 6 1986 2019
dbSNP: rs121918082
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.840 0.971 4 1986 2019
dbSNP: rs121918075
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.830 1.000 3 1986 2014
dbSNP: rs121918069
rs121918069
TTR
0.925 0.200 18 31595152 missense variant T/A;G snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.820 1.000 2 1986 2016
dbSNP: rs11541796
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1994 2014
dbSNP: rs121918068
rs121918068
TTR
0.882 0.200 18 31592983 missense variant T/A;C snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1986 2017
dbSNP: rs121918079
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1986 2014
dbSNP: rs121918080
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1986 2014
dbSNP: rs121918081
rs121918081
TTR
0.925 0.200 18 31595124 missense variant A/G snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1986 2017
dbSNP: rs121918090
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1986 2016
dbSNP: rs79977247
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.810 1.000 1 1986 2014
dbSNP: rs1800458
rs1800458
TTR
0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.020 0.500 2 2015 2016
dbSNP: rs121918095
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.010 1.000 1 2002 2002
dbSNP: rs28933981
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.010 1.000 1 1995 1995
dbSNP: rs72922940
rs72922940
TTR
0.925 0.160 18 31590735 intron variant A/G snv 9.8E-02
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
0.010 1.000 1 2015 2015