rs28933979
|
0.587 |
0.600 |
18 |
31592974 |
missense variant |
G/A;C
|
snv
|
1.0E-04
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.900 |
0.989 |
88 |
1984 |
2019 |
rs267607161
|
0.742 |
0.360 |
18 |
31598580 |
missense variant |
G/T
|
snv
|
4.0E-06
|
7.0E-06
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.870 |
1.000 |
38 |
1986 |
2020 |
rs76992529
|
0.653 |
0.560 |
18 |
31598655 |
missense variant |
G/A
|
snv
|
1.1E-03
|
4.9E-03
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.860 |
1.000 |
44 |
1986 |
2019 |
rs121918082
|
0.827 |
0.280 |
18 |
31595244 |
missense variant |
G/C
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.840 |
0.971 |
34 |
1986 |
2019 |
rs121918075
|
0.752 |
0.280 |
18 |
31598632 |
missense variant |
A/G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.830 |
1.000 |
27 |
1986 |
2014 |
rs121918069
|
0.925 |
0.200 |
18 |
31595152 |
missense variant |
T/A;G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.820 |
1.000 |
35 |
1986 |
2016 |
rs121918090
|
0.790 |
0.240 |
18 |
31593026 |
missense variant |
G/C
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
26 |
1986 |
2016 |
rs121918068
|
0.882 |
0.200 |
18 |
31592983 |
missense variant |
T/A;C
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
23 |
1986 |
2017 |
rs121918079
|
0.790 |
0.280 |
18 |
31595143 |
missense variant |
T/C
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
23 |
1986 |
2014 |
rs121918080
|
0.827 |
0.240 |
18 |
31595128 |
missense variant |
G/A;T
|
snv
|
2.4E-05
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
23 |
1986 |
2014 |
rs121918081
|
0.925 |
0.200 |
18 |
31595124 |
missense variant |
A/G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
23 |
1986 |
2017 |
rs79977247
|
0.776 |
0.200 |
18 |
31592975 |
missense variant |
T/C;G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
23 |
1986 |
2014 |
rs11541796
|
0.807 |
0.280 |
18 |
31593011 |
missense variant |
A/G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.810 |
1.000 |
3 |
1994 |
2014 |
rs121918070
|
1.000 |
0.120 |
18 |
31595157 |
missense variant |
A/G
|
snv
|
4.0E-06
|
1.4E-05
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
39 |
1986 |
2015 |
rs121918085
|
0.882 |
0.160 |
18 |
31595181 |
missense variant |
A/T
|
snv
|
1.6E-05
|
3.5E-05
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
30 |
1986 |
2017 |
rs121918071
|
0.882 |
0.240 |
18 |
31595209 |
missense variant |
C/A
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
29 |
1986 |
2015 |
rs121918089
|
1.000 |
0.120 |
18 |
31598610 |
missense variant |
A/G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
29 |
1986 |
2014 |
rs121918091
|
0.882 |
0.200 |
18 |
31595169 |
missense variant |
T/C
|
snv
|
4.0E-06
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
29 |
1986 |
2016 |
rs121918098
|
0.807 |
0.200 |
18 |
31592939 |
missense variant |
A/G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
29 |
1986 |
2014 |
rs121918083
|
1.000 |
0.120 |
18 |
31592914 |
missense variant |
T/C
|
snv
|
|
7.0E-06
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
26 |
1986 |
2014 |
rs876658108
|
1.000 |
0.120 |
18 |
31598649 |
missense variant |
G/T
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
26 |
1986 |
2017 |
rs121918072
|
1.000 |
0.120 |
18 |
31595230 |
missense variant |
T/G
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
25 |
1986 |
2014 |
rs121918100
|
0.827 |
0.160 |
18 |
31595184 |
missense variant |
T/C
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
25 |
1986 |
2015 |
rs104894665
|
0.851 |
0.120 |
18 |
31593017 |
missense variant |
T/C
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
22 |
1986 |
2014 |
rs121918073
|
0.882 |
0.160 |
18 |
31598622 |
missense variant |
C/A
|
snv
|
|
|
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
22 |
1986 |
2014 |