Have questions? Visit https://www.reddit.com/r/SNPedia

rs183211

From SNPedia

Orientationplus
Stabilizedplus
Make rs183211(A;A)
Make rs183211(A;G)
Make rs183211(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position46710944
GeneNSF
is asnp
is mentioned by
dbSNPrs183211
ebirs183211
HLIrs183211
Exacrs183211
Varsomers183211
Maprs183211
PheGenIrs183211
hapmaprs183211
1000 genomesrs183211
hgdprs183211
ensemblrs183211
gopubmedrs183211
geneviewrs183211
scholarrs183211
googlers183211
pharmgkbrs183211
gwascentralrs183211
openSNPrs183211
23andMers183211
23andMe allrs183211
SNP Nexus

SNPshotrs183211
SNPdbers183211
MSV3drs183211
GWAS Ctlgrs183211
GMAF0.4146
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21812969OA-icon.png]
Trait
Title Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
Risk Allele T
P-val 3E-7
Odds Ratio None None
GWAS snp
PMID [PMID 23544013OA-icon.png]
Trait Ovarian cancer in BRCA1 mutation carriers
Title Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Risk Allele A
P-val 3E-8
Odds Ratio 1.25 [1.16-1.35]