B2M, beta-2-microglobulin, 567

N. diseases: 352; N. variants: 6
Disease: Amyloidosis, familial visceral ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398122820
rs398122820
Entrez Id: 567
Gene Symbol: B2M
B2M
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.800 GeneticVariation UNIPROT Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin. 22693999 2012
dbSNP: rs398122820
rs398122820
Entrez Id: 567
Gene Symbol: B2M
B2M
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		A 0.800 CausalMutation CLINVAR