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rs7919006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs7919006(C;T)
Make rs7919006(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position75049002
GeneDUPD1
is asnp
is mentioned by
dbSNPrs7919006
ebirs7919006
HLIrs7919006
Exacrs7919006
Varsomers7919006
Maprs7919006
PheGenIrs7919006
hapmaprs7919006
1000 genomesrs7919006
hgdprs7919006
ensemblrs7919006
gopubmedrs7919006
geneviewrs7919006
scholarrs7919006
googlers7919006
pharmgkbrs7919006
gwascentralrs7919006
openSNPrs7919006
23andMers7919006
23andMe allrs7919006
SNP Nexus

SNPshotrs7919006
SNPdbers7919006
MSV3drs7919006
GWAS Ctlgrs7919006
GMAF0.2374
Max Magnitude0
? (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 0.000004
Odds Ratio 4.00 [NR] kg decrease


GET Evidence
rs7919006
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.234375
summary