Gene: MEN1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386134256
rs386134256
MEN1
G 0.800 CausalMutation CLINVAR Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1. 25824098

2015
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: 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: rs767319284
rs767319284
MEN1 ; MAP4K2
CG 0.700 CausalMutation CLINVAR Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotype. 22470073

2012
dbSNP: rs794728625
rs794728625
MEN1
T 0.700 CausalMutation CLINVAR Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotype. 22470073

2012
dbSNP: rs794728654
rs794728654
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotype. 22470073

2012
dbSNP: rs794728657
rs794728657
MEN1
C 0.700 CausalMutation CLINVAR Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotype. 22470073

2012
dbSNP: rs398124435
rs398124435
MEN1 ; MAP4K2
A 0.800 GeneticVariation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs104894257
rs104894257
MEN1
T 0.700 CausalMutation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs104894261
rs104894261
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs397515385
rs397515385
MEN1
T 0.700 CausalMutation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs587776841
rs587776841
MEN1
T 0.700 CausalMutation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs794728639
rs794728639
MEN1
A 0.700 CausalMutation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs794728657
rs794728657
MEN1
C 0.700 CausalMutation CLINVAR Positional cloning of the gene for multiple endocrine neoplasia-type 1. 9103196

1997
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
T 0.800 CausalMutation CLINVAR Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study. 11836268

2002
dbSNP: rs1060499974
rs1060499974
MEN1 ; MAP4K2
A 0.700 CausalMutation CLINVAR Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study. 11836268

2002
dbSNP: rs1114167489
rs1114167489
MEN1
T 0.700 CausalMutation CLINVAR Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study. 11836268

2002
dbSNP: rs1114167536
rs1114167536
MEN1 ; MAP4K2
CCCACGGCT 0.700 CausalMutation CLINVAR Parathyroid carcinoma in multiple endocrine neoplasia type 1 with a classic germline mutation. 19491073

2010
dbSNP: rs1555165488
rs1555165488
MEN1
GAAGCTCC 0.700 GeneticVariation CLINVAR Pancreatic hemi-agenesis in MEN1: A clinical report. 29174091

2018
dbSNP: rs794728615
rs794728615
MEN1
A 0.710 CausalMutation CLINVAR p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation? 24997771

2014
dbSNP: rs1060499991
rs1060499991
MEN1 ; MAP4K2
T 0.710 CausalMutation CLINVAR Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain. 22026581

2012
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