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rs12799172

From SNPedia

Orientationplus
Stabilizedplus
Make rs12799172(C;C)
Make rs12799172(C;T)
Make rs12799172(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position6728826
is asnp
is mentioned by
dbSNPrs12799172
ebirs12799172
HLIrs12799172
Exacrs12799172
Varsomers12799172
Maprs12799172
PheGenIrs12799172
hapmaprs12799172
1000 genomesrs12799172
hgdprs12799172
ensemblrs12799172
gopubmedrs12799172
geneviewrs12799172
scholarrs12799172
googlers12799172
pharmgkbrs12799172
gwascentralrs12799172
openSNPrs12799172
23andMers12799172
23andMe allrs12799172
SNP Nexus

SNPshotrs12799172
SNPdbers12799172
MSV3drs12799172
GWAS Ctlgrs12799172
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24347629OA-icon.png]
Trait Periodontal disease-related phenotypes
Title Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.
Risk Allele
P-val 5E-6
Odds Ratio 2.12 [NR]