Gene: MEN1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555165488
rs1555165488
MEN1
GAAGCTCC 0.700 GeneticVariation CLINVAR Pancreatic hemi-agenesis in MEN1: A clinical report. 29174091

2018
dbSNP: rs864622615
rs864622615
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. 29036195

2017
dbSNP: rs1565646772
rs1565646772
MEN1
A 0.700 CausalMutation CLINVAR Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years. 26767918

2016
dbSNP: rs1060499974
rs1060499974
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1. 25824098

2015
dbSNP: rs767319284
rs767319284
MEN1 ; MAP4K2
CG 0.700 CausalMutation CLINVAR Ectopic adrenocorticotropic hormone and corticotropin-releasing hormone co-secreting tumors in children and adolescents causing cushing syndrome: a diagnostic dilemma and how to solve it. 25291050

2015
dbSNP: rs794728654
rs794728654
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1. 25824098

2015
dbSNP: rs104894261
rs104894261
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation. 24218143

2014
dbSNP: rs1555166365
rs1555166365
MEN1
T 0.700 CausalMutation CLINVAR Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. 25309785

2014
dbSNP: rs1555166609
rs1555166609
MEN1
GGGGCT 0.700 CausalMutation CLINVAR Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. 25309785

2014
dbSNP: rs1555166609
rs1555166609
MEN1
GGGGCT 0.700 CausalMutation CLINVAR Multiple endocrine neoplasia type 1 associated with breast cancer: A case report and review of the literature. 24959251

2014
dbSNP: rs587776841
rs587776841
MEN1
T 0.700 CausalMutation CLINVAR Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. 25309785

2014
dbSNP: rs587776841
rs587776841
MEN1
T 0.700 CausalMutation CLINVAR Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients. 24599222

2014
dbSNP: rs587776841
rs587776841
MEN1
T 0.700 CausalMutation CLINVAR Natural course and survival of neuroendocrine tumors of thymus and lung in MEN1 patients. 24915123

2014
dbSNP: rs750904332
rs750904332
MEN1
C 0.700 CausalMutation CLINVAR Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. 25309785

2014
dbSNP: rs767319284
rs767319284
MEN1 ; MAP4K2
CG 0.700 CausalMutation CLINVAR Natural course and survival of neuroendocrine tumors of thymus and lung in MEN1 patients. 24915123

2014
dbSNP: rs794728640
rs794728640
MEN1
A 0.700 CausalMutation CLINVAR Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. 25309785

2014
dbSNP: rs864622615
rs864622615
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. 25309785

2014
dbSNP: rs587776841
rs587776841
MEN1
T 0.700 CausalMutation CLINVAR MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism. 23093699

2013
dbSNP: rs767319284
rs767319284
MEN1 ; MAP4K2
CG 0.700 CausalMutation CLINVAR Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis. 23321498

2013
dbSNP: rs767319284
rs767319284
MEN1 ; MAP4K2
C 0.700 CausalMutation CLINVAR Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis. 23321498

2013
dbSNP: rs1114167482
rs1114167482
MEN1
T 0.700 CausalMutation CLINVAR Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain. 22026581

2012
dbSNP: rs1555166609
rs1555166609
MEN1
GGGGCT 0.700 CausalMutation CLINVAR Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain. 22026581

2012
dbSNP: rs730882136
rs730882136
MEN1
GGGGGC 0.700 CausalMutation CLINVAR Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain. 22026581

2012
dbSNP: rs750904332
rs750904332
MEN1
T 0.700 CausalMutation CLINVAR Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain. 22026581

2012
dbSNP: rs750904332
rs750904332
MEN1
C 0.700 CausalMutation CLINVAR Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain. 22026581

2012