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rs1458095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1458095(C;T)
Make rs1458095(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position81274505
is asnp
is mentioned by
dbSNPrs1458095
ebirs1458095
HLIrs1458095
Exacrs1458095
Varsomers1458095
Maprs1458095
PheGenIrs1458095
hapmaprs1458095
1000 genomesrs1458095
hgdprs1458095
ensemblrs1458095
gopubmedrs1458095
geneviewrs1458095
scholarrs1458095
googlers1458095
pharmgkbrs1458095
gwascentralrs1458095
openSNPrs1458095
23andMers1458095
23andMe allrs1458095
SNP Nexus

SNPshotrs1458095
SNPdbers1458095
MSV3drs1458095
GWAS Ctlgrs1458095
GMAF0.2043
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 0.000007
Odds Ratio 0.19 [NR] kg increase


GET Evidence
rs1458095
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.210938
summary