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rs11659841

From SNPedia

Orientationplus
Stabilizedplus
Make rs11659841(C;C)
Make rs11659841(C;T)
Make rs11659841(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position28206916
is asnp
is mentioned by
dbSNPrs11659841
ebirs11659841
HLIrs11659841
Exacrs11659841
Varsomers11659841
Maprs11659841
PheGenIrs11659841
hapmaprs11659841
1000 genomesrs11659841
hgdprs11659841
ensemblrs11659841
gopubmedrs11659841
geneviewrs11659841
scholarrs11659841
googlers11659841
pharmgkbrs11659841
gwascentralrs11659841
openSNPrs11659841
23andMers11659841
23andMe allrs11659841
SNP Nexus

SNPshotrs11659841
SNPdbers11659841
MSV3drs11659841
GWAS Ctlgrs11659841
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 9E-6
Odds Ratio 2.48 [NR]