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rs2395163

From SNPedia

Orientationplus
Stabilizedplus
Make rs2395163(C;C)
Make rs2395163(C;T)
Make rs2395163(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32420032
is asnp
is mentioned by
dbSNPrs2395163
dbSNP (classic)rs2395163
ClinGenrs2395163
ebirs2395163
HLIrs2395163
Exacrs2395163
Gnomadrs2395163
Varsomers2395163
LitVarrs2395163
Maprs2395163
PheGenIrs2395163
Biobankrs2395163
1000 genomesrs2395163
hgdprs2395163
ensemblrs2395163
geneviewrs2395163
scholarrs2395163
googlers2395163
pharmgkbrs2395163
gwascentralrs2395163
openSNPrs2395163
23andMers2395163
SNPshotrs2395163
SNPdbers2395163
MSV3drs2395163
GWAS Ctlgrs2395163
GMAF0.1501
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22451204OA-icon.png]
Trait
Title Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Risk Allele
P-val 3E-11
Odds Ratio 1.2400 None

[PMID 20017995OA-icon.png] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.

[PMID 20018025OA-icon.png] Genome-wide analysis of haplotype interaction for the data from the North American Rheumatoid Arthritis Consortium.

[PMID 20018053OA-icon.png] A genome-wide association scan for rheumatoid arthritis data by Hotelling's T2 tests.


[PMID 24183452OA-icon.png] Association of Parkinson Disease with Structural and Regulatory Variants in the HLA Region