rs1057519806, MAP2K2

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
0.710 GeneticVariation BEFREE We report on a fourth familial case with transmission of CFC syndrome from father to son due to a novel heterozygous sequence change c.376A>G (p.N126D) in exon 3 of MEK2 gene. 25487361 2015
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
0.710 GeneticVariation CLINVAR
melanoma
CUI: C0025202
Disease: melanoma
0.700 GeneticVariation CLINVAR The genetic landscape of clinical resistance to RAF inhibition in metastatic melanoma. 24265153 2014
CARDIOFACIOCUTANEOUS SYNDROME 4
CUI: C3809007
Disease: CARDIOFACIOCUTANEOUS SYNDROME 4
0.700 CausalMutation CLINVAR