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rs10172965

From SNPedia

Orientationplus
Stabilizedplus
Make rs10172965(C;C)
Make rs10172965(C;T)
Make rs10172965(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position195007095
is asnp
is mentioned by
dbSNPrs10172965
ClinGenrs10172965
ebirs10172965
HLIrs10172965
Exacrs10172965
Varsomers10172965
Maprs10172965
PheGenIrs10172965
hapmaprs10172965
1000 genomesrs10172965
hgdprs10172965
ensemblrs10172965
gopubmedrs10172965
geneviewrs10172965
scholarrs10172965
googlers10172965
pharmgkbrs10172965
gwascentralrs10172965
openSNPrs10172965
23andMers10172965
23andMe allrs10172965
SNP Nexus

SNPshotrs10172965
SNPdbers10172965
MSV3drs10172965
GWAS Ctlgrs10172965
GMAF0.3163
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22832960OA-icon.png]
Trait
Title A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.
Risk Allele T
P-val 0.000006
Odds Ratio 0.3000 None