rs11080466
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Non-Small Cell Lung Carcinoma
|
C |
0.800 |
GeneticVariation |
GWASCAT |
The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.
|
21866343 |
2012 |
rs11080466
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Non-Small Cell Lung Carcinoma
|
C |
0.800 |
GeneticVariation |
GWASDB |
The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.
|
21866343 |
2012 |
rs587777076
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs587777076
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777076
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis.
|
23487782 |
2013 |
rs587777450
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
|
T |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777450
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777451
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
MARDEN-WALKER SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777451
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
MARDEN-WALKER SYNDROME
|
A |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777452
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
G |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777452
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777452
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis.
|
23487782 |
2013 |
rs587777452
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
A |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777453
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777453
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
C |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777453
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis.
|
23487782 |
2013 |
rs587777454
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs587777454
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
|
0.800 |
GeneticVariation |
UNIPROT |
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis.
|
23487782 |
2013 |
rs587777454
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Oculomelic amyoplasia
|
G |
0.800 |
CausalMutation |
CLINVAR |
Mutations in PIEZO2 cause Gordon syndrome, Marden-Walker syndrome, and distal arthrogryposis type 5.
|
24726473 |
2014 |
rs886039823
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs886039823
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1057519425
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057519426
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
|
TTCG |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057519626
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs11665020
|
Entrez Id: |
63895 |
Gene Symbol: |
PIEZO2 |
PIEZO2
|
Diastolic blood pressure
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
|
30224653 |
2018 |