SEMA5A, semaphorin 5A, 9037

N. diseases: 85; N. variants: 24
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7702187
rs7702187
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0030567
Disease:
Parkinson Disease 		0.020 GeneticVariation BEFREE Meta analysis of the association of rs7702187 SNP in SEMA5A gene with risk of Parkinson's disease. 24706317 2014
dbSNP: rs7702187
rs7702187
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0030567
Disease:
Parkinson Disease 		0.020 GeneticVariation BEFREE We found that the SEMA5A variant genotype (allele) of rs7702187 and rs3798097 had no association with the risk of PD in our sample. 18950607 2008
dbSNP: rs3798097
rs3798097
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE We found that the SEMA5A variant genotype (allele) of rs7702187 and rs3798097 had no association with the risk of PD in our sample. 18950607 2008
dbSNP: rs7702187
rs7702187
Entrez Id: 9037
Gene Symbol: SEMA5A
SEMA5A
CUI: C4511452
Disease:
Sporadic Parkinson disease 		0.010 GeneticVariation BEFREE It can be concluded that rs7702187 SNP in Sema5a gene is not a marker of PD risk in the studied populations. 16481103 2006