rs9309464
×
Entrez Id:
23233
Gene Symbol:
EXOC6B
EXOC6B
Meningitis, Pneumococcal
0.010
GeneticVariation
BEFREE
Our strongest signals associated with susceptibility to pneumococcal meningitis were rs139064549 on chromosome 1 in the COL11A1 gene (p = 1.51 × 10(-6); G allele OR 3.21 [95% CI 2.05-5.02]) and rs9309464 in the EXOC6B gene on chromosome 2 (p = 6.01 × 10(-5); G allele OR 0.66 [95% CI 0.54-0.81]).
27389768
2016
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
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
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
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
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
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
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
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
Encephalopathy, CTCAE 3.0
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
Microcephaly (physical finding)
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
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
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
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
Short neck
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
Osteopenia
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
Poor school performance
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
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
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
Facial asymmetry
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
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
Nystagmus
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