rs7702187

Orientation

plus

Stabilized

plus

Make rs7702187(A;A)

Make rs7702187(A;T)

Make rs7702187(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

9332169

Gene

SEMA5A

is a	snp
is	mentioned by
dbSNP	rs7702187
dbSNP (classic)	rs7702187
ClinGen	rs7702187
ebi	rs7702187
HLI	rs7702187
Exac	rs7702187
Gnomad	rs7702187
Varsome	rs7702187
LitVar	rs7702187
Map	rs7702187
PheGenI	rs7702187
Biobank	rs7702187
1000 genomes	rs7702187
hgdp	rs7702187
ensembl	rs7702187
geneview	rs7702187
scholar	rs7702187
google	rs7702187
pharmgkb	rs7702187
gwascentral	rs7702187
openSNP	rs7702187
23andMe	rs7702187
SNPshot	rs7702187
SNPdbe	rs7702187
MSV3d	rs7702187
GWAS Ctlg	rs7702187

GMAF

0.32

Max Magnitude

0

?

(A;A) (A;T) (T;T)

28

rs7702187 increases susceptibility to Parkinson's disease 1.74 times for carriers of the A allele [PMID 16252231 ]

[PMID 18950607] rs7702187 had no association with the risk of developing Parkinson's disease in a study of 340 Han Chinese patients.

GWAS
SNP	rs7702187
PubMedID	[PMID 16252231 ]
Condition	Parkinson's disease
Gene	SEMA5A
Risk Allele
pValue	8.00E-006
OR	1.74
95% CI	1.36-2.24

OMIM	168600
Desc	PARKINSON DISEASE; PD
Variant
Related	also

[PMID 16481103] Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk.

[PMID 16685660 ] Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease.

[PMID 16685661 ] Genomewide association, Parkinson disease, and PARK10.

[PMID 16685662 ] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

[PMID 16685663 ] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.

[PMID 19957501] [Correlation study of semaphorin 5a with risk of Parkinson's disease in a Chinese Han population].