Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine neoplasia-type 1 (MEN1). 11102994

2000
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1. 11134142

2000
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Molecular pathology of multiple endocrine neoplasia type I: two novel germline mutations and updated classification of mutations affecting MEN1 gene. 10617276

1999
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Germline MEN1 mutations in sixteen Japanese families with multiple endocrine neoplasia type 1 (MEN1). 10576763

1999
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases. 9888389

1999
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription. 9989505

1999
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1. 10229909

1999
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism. 9709921

1998
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Somatic mutations of the MEN1 tumor suppressor gene detected in sporadic angiofibromas. 9740255

1998
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT MEN1 gene mutations in 12 MEN1 families and their associated tumors. 9820618

1998
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
T 0.800 CausalMutation CLINVAR Characterization of mutations in patients with multiple endocrine neoplasia type 1. 9463336

1998
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders. 9683585

1998
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
0.800 GeneticVariation UNIPROT Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. 9215689

1997