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rs1927702

From SNPedia

Orientationplus
Stabilizedplus
Make rs1927702(C;C)
Make rs1927702(C;T)
Make rs1927702(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position15986718
is asnp
is mentioned by
dbSNPrs1927702
ebirs1927702
HLIrs1927702
Exacrs1927702
Varsomers1927702
Maprs1927702
PheGenIrs1927702
hapmaprs1927702
1000 genomesrs1927702
hgdprs1927702
ensemblrs1927702
gopubmedrs1927702
geneviewrs1927702
scholarrs1927702
googlers1927702
pharmgkbrs1927702
gwascentralrs1927702
openSNPrs1927702
23andMers1927702
23andMe allrs1927702
SNP Nexus

SNPshotrs1927702
SNPdbers1927702
MSV3drs1927702
GWAS Ctlgrs1927702
GMAF0.4692
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 0.000006
Odds Ratio 0.08 [NR] kg increase


GET Evidence
rs1927702
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.408163
summary