Gene: MEN1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167493
rs1114167493
MEN1
0.700 GeneticVariation UNIPROT

dbSNP: rs1114167494
rs1114167494
MEN1
0.700 GeneticVariation UNIPROT

dbSNP: rs1114167495
rs1114167495
MEN1
0.700 GeneticVariation UNIPROT

dbSNP: rs1114167515
rs1114167515
MEN1
0.700 GeneticVariation UNIPROT

dbSNP: rs141679530
rs141679530
MEN1 ; MAP4K2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555163780
rs1555163780
MEN1 ; MAP4K2
CCTCGGCCTCGGCCGCCTCGGCCT 0.700 CausalMutation CLINVAR

dbSNP: rs1555163883
rs1555163883
MEN1 ; MAP4K2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555164115
rs1555164115
MEN1 ; MAP4K2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555164430
rs1555164430
MEN1 ; MAP4K2
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1555164870
rs1555164870
MEN1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555164946
rs1555164946
MEN1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555164986
rs1555164986
MEN1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555165503
rs1555165503
MEN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555165756
rs1555165756
MEN1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555166466
rs1555166466
MEN1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555166494
rs1555166494
MEN1
GGCGGT 0.700 CausalMutation CLINVAR

dbSNP: rs1555166681
rs1555166681
MEN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565640081
rs1565640081
MEN1 ; MAP4K2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1565645563
rs1565645563
MEN1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1565651223
rs1565651223
MEN1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1565651568
rs1565651568
MEN1
CA 0.700 CausalMutation CLINVAR

dbSNP: rs386134245
rs386134245
MEN1
CA 0.700 GeneticVariation CLINVAR

dbSNP: rs386134246
rs386134246
MEN1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs386134247
rs386134247
MEN1
TC 0.700 GeneticVariation CLINVAR

dbSNP: rs386134247
rs386134247
MEN1
T 0.700 CausalMutation CLINVAR