Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131691067
rs1131691067
NF1
G 0.700 CausalMutation CLINVAR NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience. 23913538

2013
dbSNP: rs1131691067
rs1131691067
NF1
G 0.700 CausalMutation CLINVAR A highly sensitive genetic protocol to detect NF1 mutations. 21354044

2011
dbSNP: rs1131691067
rs1131691067
NF1
G 0.700 CausalMutation CLINVAR Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations. 11115850

2000