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rs7976091

From SNPedia

Orientationplus
Stabilizedplus
Make rs7976091(C;C)
Make rs7976091(C;T)
Make rs7976091(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position47910769
is asnp
is mentioned by
dbSNPrs7976091
ebirs7976091
HLIrs7976091
Exacrs7976091
Varsomers7976091
Maprs7976091
PheGenIrs7976091
hapmaprs7976091
1000 genomesrs7976091
hgdprs7976091
ensemblrs7976091
gopubmedrs7976091
geneviewrs7976091
scholarrs7976091
googlers7976091
pharmgkbrs7976091
gwascentralrs7976091
openSNPrs7976091
23andMers7976091
23andMe allrs7976091
SNP Nexus

SNPshotrs7976091
SNPdbers7976091
MSV3drs7976091
GWAS Ctlgrs7976091
GMAF0.4123
Max Magnitude

[PMID 22213340] 25-hydroxyvitamin D, vitamin D receptor gene polymorphisms, and severity of Parkinson's disease