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rs1840440

From SNPedia

Orientationplus
Stabilizedplus
Make rs1840440(C;C)
Make rs1840440(C;T)
Make rs1840440(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position25677222
is asnp
is mentioned by
dbSNPrs1840440
ebirs1840440
HLIrs1840440
Exacrs1840440
Varsomers1840440
Maprs1840440
PheGenIrs1840440
hapmaprs1840440
1000 genomesrs1840440
hgdprs1840440
ensemblrs1840440
gopubmedrs1840440
geneviewrs1840440
scholarrs1840440
googlers1840440
pharmgkbrs1840440
gwascentralrs1840440
openSNPrs1840440
23andMers1840440
23andMe allrs1840440
SNP Nexus

SNPshotrs1840440
SNPdbers1840440
MSV3drs1840440
GWAS Ctlgrs1840440
GMAF0.4761
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19851299]
Trait Weight
Title Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene
Risk Allele G
P-val 3E-7
Odds Ratio 2.16 [NR] kg increase


GET Evidence
rs1840440
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.390625
summary