Have questions? Visit https://www.reddit.com/r/SNPedia

rs10492096

From SNPedia

Orientationminus
Stabilizedminus
Make rs10492096(C;C)
Make rs10492096(C;T)
Make rs10492096(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position6471416
GeneVAMP1
is asnp
is mentioned by
dbSNPrs10492096
ebirs10492096
HLIrs10492096
Exacrs10492096
Varsomers10492096
Maprs10492096
PheGenIrs10492096
hapmaprs10492096
1000 genomesrs10492096
hgdprs10492096
ensemblrs10492096
gopubmedrs10492096
geneviewrs10492096
scholarrs10492096
googlers10492096
pharmgkbrs10492096
gwascentralrs10492096
openSNPrs10492096
23andMers10492096
23andMe allrs10492096
SNP Nexus

SNPshotrs10492096
SNPdbers10492096
MSV3drs10492096
GWAS Ctlgrs10492096
GMAF0.1079
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Hip geometry
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs10492096
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.140625
summary