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rs824931

From SNPedia

Orientationplus
Stabilizedplus
Make rs824931(C;C)
Make rs824931(C;T)
Make rs824931(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position221936980
is asnp
is mentioned by
dbSNPrs824931
ebirs824931
HLIrs824931
Exacrs824931
Varsomers824931
Maprs824931
PheGenIrs824931
hapmaprs824931
1000 genomesrs824931
hgdprs824931
ensemblrs824931
gopubmedrs824931
geneviewrs824931
scholarrs824931
googlers824931
pharmgkbrs824931
gwascentralrs824931
openSNPrs824931
23andMers824931
23andMe allrs824931
SNP Nexus

SNPshotrs824931
SNPdbers824931
MSV3drs824931
GWAS Ctlgrs824931
GMAF0.4444
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 0.000003
Odds Ratio 0.07 [NR] kg increase


GET Evidence
rs824931
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary