rs104894910
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs104894911
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs62637020
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637020
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637021
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs62637023
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637023
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637024
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637024
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637025
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637025
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637026
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637026
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637027
|
|
AA |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs62637027
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637027
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637028
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637028
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637030
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637030
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637032
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637032
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637033
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |
rs62637033
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
|
11062472 |
2000 |
rs62637034
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
|
11062471 |
2000 |