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rs10145182

From SNPedia

Orientationplus
Stabilizedplus
Make rs10145182(A;A)
Make rs10145182(A;T)
Make rs10145182(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position50809291
GeneNIN
is asnp
is mentioned by
dbSNPrs10145182
ebirs10145182
HLIrs10145182
Exacrs10145182
Varsomers10145182
Maprs10145182
PheGenIrs10145182
hapmaprs10145182
1000 genomesrs10145182
hgdprs10145182
ensemblrs10145182
gopubmedrs10145182
geneviewrs10145182
scholarrs10145182
googlers10145182
pharmgkbrs10145182
gwascentralrs10145182
openSNPrs10145182
23andMers10145182
23andMe allrs10145182
SNP Nexus

SNPshotrs10145182
SNPdbers10145182
MSV3drs10145182
GWAS Ctlgrs10145182
GMAF0.2328
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 20056645OA-icon.png] Association of mitotic regulation pathway polymorphisms with pancreatic cancer risk and outcome


[PMID 20508983OA-icon.png] Centrosome-related genes, genetic variation, and risk of breast cancer