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rs1474747

From SNPedia

Orientationplus
Stabilizedplus
Make rs1474747(C;C)
Make rs1474747(C;T)
Make rs1474747(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159178723
GeneCADM3
is asnp
is mentioned by
dbSNPrs1474747
ebirs1474747
HLIrs1474747
Exacrs1474747
Varsomers1474747
Maprs1474747
PheGenIrs1474747
hapmaprs1474747
1000 genomesrs1474747
hgdprs1474747
ensemblrs1474747
gopubmedrs1474747
geneviewrs1474747
scholarrs1474747
googlers1474747
pharmgkbrs1474747
gwascentralrs1474747
openSNPrs1474747
23andMers1474747
23andMe allrs1474747
SNP Nexus

SNPshotrs1474747
SNPdbers1474747
MSV3drs1474747
GWAS Ctlgrs1474747
GMAF0.3287
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.0000030000000000000001
Odds Ratio NR NR


GET Evidence
rs1474747
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.609375
summary