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rs10089

From SNPedia

Orientationplus
Stabilizedplus
Make rs10089(C;C)
Make rs10089(C;T)
Make rs10089(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position128186851
GeneSLC12A2
is asnp
is mentioned by
dbSNPrs10089
ebirs10089
HLIrs10089
Exacrs10089
Varsomers10089
Maprs10089
PheGenIrs10089
hapmaprs10089
1000 genomesrs10089
hgdprs10089
ensemblrs10089
gopubmedrs10089
geneviewrs10089
scholarrs10089
googlers10089
pharmgkbrs10089
gwascentralrs10089
openSNPrs10089
23andMers10089
23andMe allrs10089
SNP Nexus

SNPshotrs10089
SNPdbers10089
MSV3drs10089
GWAS Ctlgrs10089
GMAF0.2461
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21139019OA-icon.png]
Trait
Title A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum
Risk Allele
P-val 0.000002
Odds Ratio 2.5600 [1.79-3.70]


[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.