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rs10176394

From SNPedia

Orientationplus
Stabilizedplus
Make rs10176394(C;C)
Make rs10176394(C;T)
Make rs10176394(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position143338805
GeneARHGAP15
is asnp
is mentioned by
dbSNPrs10176394
ebirs10176394
HLIrs10176394
Exacrs10176394
Varsomers10176394
Maprs10176394
PheGenIrs10176394
hapmaprs10176394
1000 genomesrs10176394
hgdprs10176394
ensemblrs10176394
gopubmedrs10176394
geneviewrs10176394
scholarrs10176394
googlers10176394
pharmgkbrs10176394
gwascentralrs10176394
openSNPrs10176394
23andMers10176394
23andMe allrs10176394
SNP Nexus

SNPshotrs10176394
SNPdbers10176394
MSV3drs10176394
GWAS Ctlgrs10176394
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24556642OA-icon.png]
Trait Smooth-surface caries
Title Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.
Risk Allele T
P-val 2E-6
Odds Ratio 1.77 [NR] unit decrease