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rs10849373

From SNPedia

Orientationplus
Stabilizedplus
Make rs10849373(A;A)
Make rs10849373(A;G)
Make rs10849373(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position631795
GeneNINJ2, PPIAP21
is asnp
is mentioned by
dbSNPrs10849373
ebirs10849373
HLIrs10849373
Exacrs10849373
Varsomers10849373
Maprs10849373
PheGenIrs10849373
hapmaprs10849373
1000 genomesrs10849373
hgdprs10849373
ensemblrs10849373
gopubmedrs10849373
geneviewrs10849373
scholarrs10849373
googlers10849373
pharmgkbrs10849373
gwascentralrs10849373
openSNPrs10849373
23andMers10849373
23andMe allrs10849373
SNP Nexus

SNPshotrs10849373
SNPdbers10849373
MSV3drs10849373
GWAS Ctlgrs10849373
GMAF0.2544
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21722921] NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population