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rs7118648

From SNPedia

Orientationplus
Stabilizedplus
Make rs7118648(C;C)
Make rs7118648(C;T)
Make rs7118648(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position96375264
GeneCCDC82
is asnp
is mentioned by
dbSNPrs7118648
dbSNP (old)rs7118648
ClinGenrs7118648
ebirs7118648
HLIrs7118648
Exacrs7118648
Gnomadrs7118648
Varsomers7118648
Maprs7118648
PheGenIrs7118648
Biobankrs7118648
1000 genomesrs7118648
hgdprs7118648
ensemblrs7118648
gopubmedrs7118648
geneviewrs7118648
scholarrs7118648
googlers7118648
pharmgkbrs7118648
gwascentralrs7118648
openSNPrs7118648
23andMers7118648
23andMe allrs7118648
SNP Nexus

SNPshotrs7118648
SNPdbers7118648
MSV3drs7118648
GWAS Ctlgrs7118648
GMAF0.06566
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23793441OA-icon.png]
Trait Parkinson's disease
Title Parkinson disease loci in the mid-western Amish.
Risk Allele G
P-val 2E-7
Odds Ratio NR NR