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rs9291683

From SNPedia

Orientationplus
Stabilizedplus
Make rs9291683(A;A)
Make rs9291683(A;G)
Make rs9291683(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position10322536
is asnp
is mentioned by
dbSNPrs9291683
ebirs9291683
HLIrs9291683
Exacrs9291683
Varsomers9291683
Maprs9291683
PheGenIrs9291683
hapmaprs9291683
1000 genomesrs9291683
hgdprs9291683
ensemblrs9291683
gopubmedrs9291683
geneviewrs9291683
scholarrs9291683
googlers9291683
pharmgkbrs9291683
gwascentralrs9291683
openSNPrs9291683
23andMers9291683
23andMe allrs9291683
SNP Nexus

SNPshotrs9291683
SNPdbers9291683
MSV3drs9291683
GWAS Ctlgrs9291683
GMAF0.3921
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Bone mineral density
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 0.0000019999999999999999
Odds Ratio NR NR


[PMID 21276240OA-icon.png] A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study.


GET Evidence
rs9291683
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary