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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
dbSNP (classic)rs2383393
ClinGenrs2383393
ebirs2383393
HLIrs2383393
Exacrs2383393
Gnomadrs2383393
Varsomers2383393
LitVarrs2383393
Maprs2383393
PheGenIrs2383393
Biobankrs2383393
1000 genomesrs2383393
hgdprs2383393
ensemblrs2383393
geneviewrs2383393
scholarrs2383393
googlers2383393
pharmgkbrs2383393
gwascentralrs2383393
openSNPrs2383393
23andMers2383393
SNPshotrs2383393
SNPdbers2383393
MSV3drs2383393
GWAS Ctlgrs2383393
GMAF0.2934
Max Magnitude0
? (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