rs138952094
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
Delayed Puberty
A
0.700
GeneticVariation
CLINVAR
rs143007146
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
Malignant neoplasm of breast
0.700
GeneticVariation
UNIPROT
rs199979628
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
rs7804122
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
Hirschsprung Disease
0.010
GeneticVariation
BEFREE
Our results for rs7804122 provided preliminary evidence that the SEMA3A gene is involved in the susceptibility to HSCR in the Northeastern Chinese population.
22184102
2012
rs797821
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
Hirschsprung Disease
0.010
GeneticVariation
BEFREE
The genotypes of two SNPs (rs7804122 and rs797821 ) in the SEMA3A gene in 119 patients with HSCR and 93 controls were examined using PCR-sequencing to determine the contribution of SEMA3A to the HSCR phenotype.
22184102
2012
rs137871935
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs139295139
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs318240751
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs318240752
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs318240753
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs36026860
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs748219597
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs761486957
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development.
22416012
2012
rs137871935
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs139295139
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs318240751
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs318240752
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs318240753
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs36026860
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs748219597
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs761486957
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
22927827
2012
rs138694505
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
Cardiac Arrest
0.010
GeneticVariation
BEFREE
A high incidence of SEMA3A(I334V ) in UCA patients and inappropriate innervation patterning in their hearts implicate involvement of the SEMA3A gene in the pathogenesis of UCA.
23593010
2013
rs147436181
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
Kaposi Sarcoma
0.010
GeneticVariation
BEFREE
Three heterozygous variants (c.458A>G (p.Asn153Ser), c.1253A>G (p.Asn418Ser), and c.1303G>A (p.Val435Ile )) were found in SEMA3A in three KS patients, two of which also had a mutation in FGFR1.
24522099
2014
rs137871935
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.
25077900
2014
rs139295139
×
Entrez Id:
10371
Gene Symbol:
SEMA3A
SEMA3A
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA
0.700
GeneticVariation
UNIPROT
The prevalence of CHD7 missense versus truncating mutations is higher in patients with Kallmann syndrome than in typical CHARGE patients.
25077900
2014