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rs78015699

From SNPedia

Orientationplus
Stabilizedplus
Make rs78015699(C;C)
Make rs78015699(C;T)
Make rs78015699(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position18376857
is asnp
is mentioned by
dbSNPrs78015699
ebirs78015699
HLIrs78015699
Exacrs78015699
Varsomers78015699
Maprs78015699
PheGenIrs78015699
hapmaprs78015699
1000 genomesrs78015699
hgdprs78015699
ensemblrs78015699
gopubmedrs78015699
geneviewrs78015699
scholarrs78015699
googlers78015699
pharmgkbrs78015699
gwascentralrs78015699
openSNPrs78015699
23andMers78015699
23andMe allrs78015699
SNP Nexus

SNPshotrs78015699
SNPdbers78015699
MSV3drs78015699
GWAS Ctlgrs78015699
Max Magnitude
GWAS snp
PMID [PMID 24024966]
Trait Periodontitis (Mean PAL)
Title Genome-wide association study of chronic periodontitis in a general German population.
Risk Allele T
P-val 7E-6
Odds Ratio .22 [0.12-0.31] unit increase