rs138296890
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Body Height
|
|
0.700 |
GeneticVariation |
GWASCAT |
Characterizing rare and low-frequency height-associated variants in the Japanese population.
|
31562340 |
2019 |
rs10193543
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Diastolic blood pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
|
30224653 |
2018 |
rs1553417206
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Dysmorphic features
|
C |
0.700 |
GeneticVariation |
CLINVAR |
A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B gene.
|
26669664 |
2016 |
rs1553417206
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Movement Disorders
|
C |
0.700 |
GeneticVariation |
CLINVAR |
A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B gene.
|
26669664 |
2016 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Eczema
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Facial asymmetry
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Global developmental delay
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Dysmorphic facies
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Seizures
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Short stature
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Cutis marmorata
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Myopia
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Osteopenia
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Poor school performance
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Penile hypospadias
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Encephalopathy, CTCAE 3.0
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Short neck
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Nystagmus
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Torticollis
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Wide spaced nipples
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Microcephaly (physical finding)
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability.
|
25256811 |
2014 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Dysmorphic facies
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.
|
23422942 |
2013 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Torticollis
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.
|
23422942 |
2013 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Myopia
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.
|
23422942 |
2013 |
rs1064795104
|
Entrez Id: |
23233 |
Gene Symbol: |
EXOC6B |
EXOC6B
|
Cutis marmorata
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.
|
23422942 |
2013 |