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rs7749983

From SNPedia

Orientationplus
Stabilizedplus
Make rs7749983(A;A)
Make rs7749983(A;T)
Make rs7749983(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position129553210
GeneLOC102723409
is asnp
is mentioned by
dbSNPrs7749983
ebirs7749983
HLIrs7749983
Exacrs7749983
Varsomers7749983
Maprs7749983
PheGenIrs7749983
hapmaprs7749983
1000 genomesrs7749983
hgdprs7749983
ensemblrs7749983
gopubmedrs7749983
geneviewrs7749983
scholarrs7749983
googlers7749983
pharmgkbrs7749983
gwascentralrs7749983
openSNPrs7749983
23andMers7749983
23andMe allrs7749983
SNP Nexus

SNPshotrs7749983
SNPdbers7749983
MSV3drs7749983
GWAS Ctlgrs7749983
Max Magnitude
? (A;A) (A;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 2E-6
Odds Ratio 2.39 [NR]