rs779248881
MCM3AP;MCM3AP-AS1
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.800
GeneticVariation
UNIPROT
rs779248881
MCM3AP;MCM3AP-AS1
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
T
0.800
CausalMutation
CLINVAR
rs1569086477
MCM3AP;YBEY
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
A
0.700
CausalMutation
CLINVAR
rs773228537
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Colorectal Carcinoma
0.700
GeneticVariation
UNIPROT
rs373674344
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
29982295
2018
rs483352869
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
29982295
2018
rs779630101
MCM3AP;MCM3AP-AS1
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
29982295
2018
rs373674344
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation.
28969388
2017
rs483352869
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation.
28969388
2017
rs779630101
MCM3AP;MCM3AP-AS1
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation.
28969388
2017
rs149024257
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Blood Protein Measurement
G
0.700
GeneticVariation
GWASCAT
Co-regulatory networks of human serum proteins link genetics to disease.
30072576
2018
rs2839186
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Testicular Germ Cell Tumor
T
0.800
GeneticVariation
GWASCAT
Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor.
28604728
2017
rs2839186
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Testicular Germ Cell Tumor
T
0.800
GeneticVariation
GWASDB
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.
23666240
2013
rs2839186
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Testicular Neoplasms
T
0.700
GeneticVariation
GWASCAT
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.
23666240
2013
rs373674344
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
24123876
2013
rs483352869
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
24123876
2013
rs779630101
MCM3AP;MCM3AP-AS1
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
24123876
2013
rs373674344
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
28633435
2017
rs483352869
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
28633435
2017
rs779630101
MCM3AP;MCM3AP-AS1
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
0.700
GeneticVariation
UNIPROT
MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
28633435
2017
rs9982623
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Periodontitis
C
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci.
30218097
2019
rs9982623
×
Entrez Id:
8888
Gene Symbol:
MCM3AP
MCM3AP
Periodontosis
C
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci.
30218097
2019
rs2839168
MCM3AP;MCM3AP-AS1
Lymphocyte Count measurement
0.700
GeneticVariation
GWASDB
The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.
22286170
2012
rs2839178
MCM3AP;MCM3AP-AS1
Breast Carcinoma
0.010
GeneticVariation
BEFREE
The G allele of rs2839178 at the GANP locus was significantly associated with reduced breast cancer risk and longer DFS in breast cancer patients, showing a consistent direction in the association between susceptibility and clinical outcome.
30810967
2019
rs2839178
MCM3AP;MCM3AP-AS1
Malignant neoplasm of breast
0.010
GeneticVariation
BEFREE
The G allele of rs2839178 at the GANP locus was significantly associated with reduced breast cancer risk and longer DFS in breast cancer patients, showing a consistent direction in the association between susceptibility and clinical outcome.
30810967
2019