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rs7617877

From SNPedia

Orientationplus
Stabilizedplus
Make rs7617877(A;A)
Make rs7617877(A;G)
Make rs7617877(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position28664273
GeneCCDC61
is asnp
is mentioned by
dbSNPrs7617877
ebirs7617877
HLIrs7617877
Exacrs7617877
Varsomers7617877
Maprs7617877
PheGenIrs7617877
hapmaprs7617877
1000 genomesrs7617877
hgdprs7617877
ensemblrs7617877
gopubmedrs7617877
geneviewrs7617877
scholarrs7617877
googlers7617877
pharmgkbrs7617877
gwascentralrs7617877
openSNPrs7617877
23andMers7617877
23andMe allrs7617877
SNP Nexus

SNPshotrs7617877
SNPdbers7617877
MSV3drs7617877
GWAS Ctlgrs7617877
GMAF0.3365
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21044948OA-icon.png]
Trait
Title Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
Risk Allele A
P-val 0.000003
Odds Ratio 1.2300 [1.13-1.33]