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rs10972341

From SNPedia

Orientationplus
Stabilizedplus
Make rs10972341(A;A)
Make rs10972341(A;G)
Make rs10972341(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position35141708
is asnp
is mentioned by
dbSNPrs10972341
ebirs10972341
HLIrs10972341
Exacrs10972341
Varsomers10972341
Maprs10972341
PheGenIrs10972341
hapmaprs10972341
1000 genomesrs10972341
hgdprs10972341
ensemblrs10972341
gopubmedrs10972341
geneviewrs10972341
scholarrs10972341
googlers10972341
pharmgkbrs10972341
gwascentralrs10972341
openSNPrs10972341
23andMers10972341
23andMe allrs10972341
SNP Nexus

SNPshotrs10972341
SNPdbers10972341
MSV3drs10972341
GWAS Ctlgrs10972341
GMAF0.4633
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000009
Odds Ratio 2.32 [NR] kg increase


GET Evidence
rs10972341
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.554688
summary