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rs2383393

From SNPedia

Orientationminus
Stabilizedminus
Make rs2383393(C;C)
Make rs2383393(C;T)
Make rs2383393(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position179743500
is asnp
is mentioned by
dbSNPrs2383393
ebirs2383393
HLIrs2383393
Exacrs2383393
Varsomers2383393
Maprs2383393
PheGenIrs2383393
hapmaprs2383393
1000 genomesrs2383393
hgdprs2383393
ensemblrs2383393
gopubmedrs2383393
geneviewrs2383393
scholarrs2383393
googlers2383393
pharmgkbrs2383393
gwascentralrs2383393
openSNPrs2383393
23andMers2383393
23andMe allrs2383393
SNP Nexus

SNPshotrs2383393
SNPdbers2383393
MSV3drs2383393
GWAS Ctlgrs2383393
GMAF0.2934
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 0.000002
Odds Ratio 0.10 [NR] kg increase


GET Evidence
rs2383393
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.674603
summary