Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Characterisation of inherited and sporadic mutations in neurofibromatosis type-1. 7981679

1994

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas. 21838856

2011

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
G 0.800 GeneticVariation CLINVAR LOVD v.2.0: the next generation in gene variant databases. 21520333

2011

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Neurofibromatosis type 1 in genetic counseling practice: recommendations of the National Society of Genetic Counselors. 17636453

2007

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT NF1 mutations and clinical spectrum in patients with spinal neurofibromas. 12746402

2003

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
G 0.800 CausalMutation CLINVAR

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Characterization and significance of nine novel mutations in exon 16 of the neurofibromatosis type 1 (NF1) gene. 9150739

1997

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
G 0.800 GeneticVariation CLINVAR Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain. 15060124

2004

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
T 0.800 CausalMutation CLINVAR NF1 mutations in neurofibromatosis 1 patients with plexiform neurofibromas. 11857752

2002

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
T 0.800 CausalMutation CLINVAR Molecular diagnosis of neurofibromatosis type 1: 2 years experience. 16944272

2007

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Disruption of exonic splicing enhancer elements is the principal cause of exon skipping associated with seven nonsense or missense alleles of NF1. 15523642

2004

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
G 0.800 GeneticVariation CLINVAR Identification of neurofibromin mutants that exhibit allele specificity or increased Ras affinity resulting in suppression of activated ras alleles. 8628317

1996

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Mutational and functional analysis of the neurofibromatosis type 1 (NF1) gene. 9003501

1997

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphisms. 8834249

1996

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
G 0.800 GeneticVariation CLINVAR Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain. 10712197

2000

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
T 0.800 CausalMutation CLINVAR Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1. 23668869

2013

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility. 20065170

2010

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Analysis of mutations at the neurofibromatosis 1 (NF1) locus. 1302608

1992

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
T 0.800 CausalMutation CLINVAR Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population. 26056819

2015

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Thirty-nine novel neurofibromatosis 1 (NF1) gene mutations identified in Slovak patients. 23758643

2013

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Neurofibromatous neuropathy in neurofibromatosis 1 (NF1). 15520408

2004

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Novel and recurrent mutations in the neurofibromatosis type 1 (NF1) gene. 9101300

1997

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
T 0.800 CausalMutation CLINVAR Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. 10862084

2000

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Six novel mutations in the neurofibromatosis type 1 (NF1) gene. 9298829

1997

dbSNP: rs199474742
rs199474742
NF1
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.800 GeneticVariation UNIPROT Selective disactivation of neurofibromin GAP activity in neurofibromatosis type 1. 9668168

1998