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rs3803915

From SNPedia

Orientationplus
Stabilizedplus
Make rs3803915(A;A)
Make rs3803915(A;C)
Make rs3803915(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position2160530
is asnp
is mentioned by
dbSNPrs3803915
ebirs3803915
HLIrs3803915
Exacrs3803915
Varsomers3803915
Maprs3803915
PheGenIrs3803915
hapmaprs3803915
1000 genomesrs3803915
hgdprs3803915
ensemblrs3803915
gopubmedrs3803915
geneviewrs3803915
scholarrs3803915
googlers3803915
pharmgkbrs3803915
gwascentralrs3803915
openSNPrs3803915
23andMers3803915
23andMe allrs3803915
SNP Nexus

SNPshotrs3803915
SNPdbers3803915
MSV3drs3803915
GWAS Ctlgrs3803915
GMAF0.1437
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 0.000005
Odds Ratio 0.13 [NR] kg decrease


GET Evidence
rs3803915
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.148438
summary



GWAS snp
PMID [PMID 24916648]
Trait Myocardial infarction
Title A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
Risk Allele C
P-val 4E-9
Odds Ratio 1.12 [1.09-1.16]