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rs1878047

From SNPedia

Orientationminus
Stabilizedminus
Make rs1878047(C;C)
Make rs1878047(C;T)
Make rs1878047(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position51270548
is asnp
is mentioned by
dbSNPrs1878047
ebirs1878047
HLIrs1878047
Exacrs1878047
Varsomers1878047
Maprs1878047
PheGenIrs1878047
hapmaprs1878047
1000 genomesrs1878047
hgdprs1878047
ensemblrs1878047
gopubmedrs1878047
geneviewrs1878047
scholarrs1878047
googlers1878047
pharmgkbrs1878047
gwascentralrs1878047
openSNPrs1878047
23andMers1878047
23andMe allrs1878047
SNP Nexus

SNPshotrs1878047
SNPdbers1878047
MSV3drs1878047
GWAS Ctlgrs1878047
GMAF0.4536
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19851299]
Trait Body mass index
Title Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene
Risk Allele G
P-val 0.000005
Odds Ratio 0.06 [NR] kg decrease


GET Evidence
rs1878047
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5625
summary