Have questions? Visit https://www.reddit.com/r/SNPedia

rs1024889

From SNPedia

Orientationplus
Stabilizedplus
Make rs1024889(A;A)
Make rs1024889(A;G)
Make rs1024889(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position70414179
is asnp
is mentioned by
dbSNPrs1024889
ebirs1024889
HLIrs1024889
Exacrs1024889
Varsomers1024889
Maprs1024889
PheGenIrs1024889
hapmaprs1024889
1000 genomesrs1024889
hgdprs1024889
ensemblrs1024889
gopubmedrs1024889
geneviewrs1024889
scholarrs1024889
googlers1024889
pharmgkbrs1024889
gwascentralrs1024889
openSNPrs1024889
23andMers1024889
23andMe allrs1024889
SNP Nexus

SNPshotrs1024889
SNPdbers1024889
MSV3drs1024889
GWAS Ctlgrs1024889
GMAF0.1795
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000006
Odds Ratio 0.12 [NR] kg increase


GET Evidence
rs1024889
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary