rs149032771
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
T
0.700
CausalMutation
CLINVAR
rs1554400338
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
T
0.700
CausalMutation
CLINVAR
rs1554490549
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
C
0.700
CausalMutation
CLINVAR
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
16571880
2006
rs201076428
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
A
0.700
CausalMutation
CLINVAR
rs371642222
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
T
0.700
CausalMutation
CLINVAR
rs398124268
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
A
0.700
CausalMutation
CLINVAR
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.
21827697
2011
rs730880275
CNTNAP2;LOC105375554
Pitt-Hopkins-Like Syndrome 1
T
0.700
CausalMutation
CLINVAR
rs730880276
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
T
0.700
CausalMutation
CLINVAR
rs752550849
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Pitt-Hopkins-Like Syndrome 1
T
0.700
CausalMutation
CLINVAR
rs771827120
CNTNAP2;LOC105375554
Pitt-Hopkins-Like Syndrome 1
C
0.700
CausalMutation
CLINVAR
rs802568
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Psychotic Disorders
0.800
GeneticVariation
GWASCAT
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs802568
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Psychotic Disorders
C
0.800
GeneticVariation
GWASDB
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs802524
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Psychotic Disorders
0.700
GeneticVariation
GWASDB
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
20889312
2010
rs2530313
CNTNAP2;LOC105375554
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018
rs10255956
×
Entrez Id:
26047
Gene Symbol:
CNTNAP2
CNTNAP2
Serum albumin measurement
0.700
GeneticVariation
GWASDB
A genome-wide assessment of variability in human serum metabolism.
23281178
2013