Rs11866328

From SNPedia
Jump to: navigation, search

Orientationplus
Make rs11866328(G;G)
Make rs11866328(G;T)
Make rs11866328(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position9768699
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs11866328
Exacrs11866328
PheGenIrs11866328
nextbiors11866328
hapmaprs11866328
1000 genomesrs11866328
hgdprs11866328
ensemblrs11866328
gopubmedrs11866328
geneviewrs11866328
scholarrs11866328
googlers11866328
pharmgkbrs11866328
gwascentralrs11866328
openSNPrs11866328
23andMers11866328
23andMe allrs11866328
SNP Nexus

SNPshotrs11866328
SNPdbers11866328
MSV3drs11866328
GMAF0.3315
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 22004137] A Genome-Wide Association Study with DNA Pooling Identifies the Variant rs11866328 in the GRIN2A Gene That Affects Disease Progression of Chronic HBV Infection