Rs10492681

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ReferenceGRCh38 38.1/141
Chromosome13
Position40233346
is asnp
is mentioned by
dbSNPrs10492681
Exacrs10492681
PheGenIrs10492681
nextbiors10492681
hapmaprs10492681
1000 genomesrs10492681
hgdprs10492681
ensemblrs10492681
gopubmedrs10492681
geneviewrs10492681
scholarrs10492681
googlers10492681
pharmgkbrs10492681
gwascentralrs10492681
openSNPrs10492681
23andMers10492681
23andMe allrs10492681
SNP Nexus

SNPshotrs10492681
SNPdbers10492681
MSV3drs10492681
GMAF0.3062
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 0.0000019999999999999999
Odds Ratio NR NR


GET Evidence
rs10492681
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary