B2M, beta-2-microglobulin, 567

N. diseases: 352; N. variants: 6
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: rs104894481
rs104894481
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C1855796
Disease:
Hypoproteinemia, Hypercatabolic 		0.800 GeneticVariation UNIPROT Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene. 16549777 2006
dbSNP: rs104894481
rs104894481
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C1855796
Disease:
Hypoproteinemia, Hypercatabolic 		C 0.800 CausalMutation CLINVAR
dbSNP: rs398122820
rs398122820
Entrez Id: 567
Gene Symbol: B2M
B2M
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		A 0.800 CausalMutation CLINVAR
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0026764
Disease:
Multiple Myeloma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0149925
Disease:
Small cell carcinoma of lung 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0279663
Disease:
Serous cystadenocarcinoma ovary 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0151779
Disease:
Cutaneous Melanoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0009404
Disease:
Colorectal Neoplasms 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0149925
Disease:
Small cell carcinoma of lung 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0152013
Disease:
Adenocarcinoma of lung (disorder) 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0151779
Disease:
Cutaneous Melanoma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1023835002
rs1023835002
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C4721532
Disease:
Lymphoma, Non-Hodgkin, Familial 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs1057519877
rs1057519877
Entrez Id: 567;197135
Gene Symbol: B2M;PATL2
B2M;PATL2
CUI: C0009404
Disease:
Colorectal Neoplasms 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016