rs121918007
|
0.851 |
0.080 |
1 |
21564139 |
missense variant |
G/A;C
|
snv
|
2.4E-03;
4.0E-06
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.710 |
1.000 |
6 |
1992 |
2014 |
rs121918001
|
0.882 |
0.080 |
1 |
21561126 |
missense variant |
C/A;T
|
snv
|
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
1.000 |
1 |
2001 |
2001 |
rs1442918125
|
0.925 |
0.080 |
1 |
21575907 |
missense variant |
G/A
|
snv
|
8.0E-06
|
7.0E-06
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
1.000 |
1 |
2001 |
2001 |
rs121918002
|
0.851 |
0.080 |
1 |
21573683 |
missense variant |
A/C
|
snv
|
3.6E-05
|
7.0E-05
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918008
|
0.851 |
0.080 |
1 |
21575868 |
missense variant |
A/T
|
snv
|
4.0E-06
|
7.0E-06
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918009
|
0.851 |
0.080 |
1 |
21575736 |
missense variant |
G/A
|
snv
|
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918011
|
0.851 |
0.080 |
1 |
21563219 |
missense variant |
G/A;C
|
snv
|
1.4E-04
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918013
|
0.827 |
0.120 |
1 |
21563158 |
missense variant |
G/A
|
snv
|
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918018
|
0.882 |
0.120 |
1 |
21568201 |
missense variant |
G/C;T
|
snv
|
1.6E-05;
4.0E-06
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918019
|
0.882 |
0.080 |
1 |
21564094 |
missense variant |
G/A;C
|
snv
|
9.2E-05
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs121918020
|
0.925 |
0.080 |
1 |
21570326 |
missense variant |
C/T
|
snv
|
1.6E-05
|
1.4E-05
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs1237252052
|
1.000 |
0.080 |
1 |
21570336 |
missense variant |
T/C
|
snv
|
4.0E-06
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs1413274209
|
0.882 |
0.080 |
1 |
21577544 |
missense variant |
G/A
|
snv
|
8.3E-06
|
2.1E-05
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs199669988
|
0.882 |
0.080 |
1 |
21564097 |
missense variant |
G/A
|
snv
|
1.3E-04
|
3.5E-05
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs371243939
|
0.882 |
0.080 |
1 |
21575906 |
missense variant |
C/T
|
snv
|
1.2E-05
|
1.4E-05
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs766076920
|
0.882 |
0.080 |
1 |
21568122 |
missense variant |
C/T
|
snv
|
8.0E-06
|
2.1E-05
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|
rs786204530
|
0.851 |
0.160 |
1 |
21563212 |
missense variant |
AC/CA
|
mnv
|
|
|
Childhood hypophosphatasia (disorder)
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
|
0.700 |
|
0 |
|
|