rs2395163
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2395163(C;C) |
Make rs2395163(C;T) |
Make rs2395163(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 32420032 |
is a | snp |
is | mentioned by |
dbSNP | rs2395163 |
dbSNP (classic) | rs2395163 |
ClinGen | rs2395163 |
ebi | rs2395163 |
HLI | rs2395163 |
Exac | rs2395163 |
Gnomad | rs2395163 |
Varsome | rs2395163 |
LitVar | rs2395163 |
Map | rs2395163 |
PheGenI | rs2395163 |
Biobank | rs2395163 |
1000 genomes | rs2395163 |
hgdp | rs2395163 |
ensembl | rs2395163 |
geneview | rs2395163 |
scholar | rs2395163 |
rs2395163 | |
pharmgkb | rs2395163 |
gwascentral | rs2395163 |
openSNP | rs2395163 |
23andMe | rs2395163 |
SNPshot | rs2395163 |
SNPdbe | rs2395163 |
MSV3d | rs2395163 |
GWAS Ctlg | rs2395163 |
GMAF | 0.1501 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22451204![]() |
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 20017995] A principal-components-based clustering method to identify multiple variants associated with rheumatoid arthritis and arthritis-related autoantibodies.
[PMID 20018025] Genome-wide analysis of haplotype interaction for the data from the North American Rheumatoid Arthritis Consortium.
[PMID 20018053] A genome-wide association scan for rheumatoid arthritis data by Hotelling's T2 tests.
[PMID 24183452] Association of Parkinson Disease with Structural and Regulatory Variants in the HLA Region
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d