Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119478058
rs119478058
Entrez Id: 81693
Gene Symbol: AMN
AMN
CUI: C4016948
Disease:
MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
T 0.700 CausalMutation CLINVAR
dbSNP: rs386834168
rs386834168
Entrez Id: 81693
Gene Symbol: AMN
AMN
CUI: C4016948
Disease:
MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
T 0.700 CausalMutation CLINVAR