SNCB, synuclein beta, 6620

N. diseases: 60; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893936
rs104893936
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
0.730 GeneticVariation BEFREE Furthermore, two missense mutations (P123H and V70M) of beta-syn were recently identified in DLB. 19711118 2009
dbSNP: rs104893937
rs104893937
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
0.730 GeneticVariation BEFREE Furthermore, two missense mutations (P123H and V70M) of beta-syn were recently identified in DLB. 19711118 2009
dbSNP: rs104893936
rs104893936
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
0.730 GeneticVariation BEFREE Two missense mutations (P123H and V70M) of beta-synuclein (beta-syn), the homologue of alpha-syn, have been recently identified in dementia with Lewy bodies. 17652097 2007
dbSNP: rs104893937
rs104893937
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
0.730 GeneticVariation BEFREE Two missense mutations (P123H and V70M) of beta-synuclein (beta-syn), the homologue of alpha-syn, have been recently identified in dementia with Lewy bodies. 17652097 2007
dbSNP: rs104893936
rs104893936
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
0.730 GeneticVariation BEFREE Two amino acid alterations were identified in unrelated DLB index cases: a valine to methionine substitution at codon 70 (V70M) and a proline to histidine substitution at codon 123 (P123H), both in the beta-synuclein gene. 15365127 2004
dbSNP: rs104893937
rs104893937
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
0.730 GeneticVariation BEFREE Two amino acid alterations were identified in unrelated DLB index cases: a valine to methionine substitution at codon 70 (V70M) and a proline to histidine substitution at codon 123 (P123H), both in the beta-synuclein gene. 15365127 2004
dbSNP: rs104893936
rs104893936
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
T 0.730 CausalMutation CLINVAR
dbSNP: rs104893937
rs104893937
Entrez Id: 6620
Gene Symbol: SNCB
SNCB
CUI: C0752347
Disease:
Lewy Body Disease
T 0.730 CausalMutation CLINVAR