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rs7077361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs7077361(C;C)
Make rs7077361(C;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position15519544
GeneITGA8
is asnp
is mentioned by
dbSNPrs7077361
ebirs7077361
HLIrs7077361
Exacrs7077361
Varsomers7077361
Maprs7077361
PheGenIrs7077361
hapmaprs7077361
1000 genomesrs7077361
hgdprs7077361
ensemblrs7077361
gopubmedrs7077361
geneviewrs7077361
scholarrs7077361
googlers7077361
pharmgkbrs7077361
gwascentralrs7077361
openSNPrs7077361
23andMers7077361
23andMe allrs7077361
SNP Nexus

SNPshotrs7077361
SNPdbers7077361
MSV3drs7077361
GWAS Ctlgrs7077361
GMAF0.06244
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19915575OA-icon.png]
Trait Parkinson's disease
Title Genome-wide association study reveals genetic risk underlying Parkinson's disease
Risk Allele C
P-val 0.000005
Odds Ratio 1.19 [NR]


GET Evidence
rs7077361
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0859375
summary