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rs1816002

From SNPedia

Orientationplus
Stabilizedplus
Make rs1816002(C;C)
Make rs1816002(C;T)
Make rs1816002(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position70723254
GeneADAMTS14
is asnp
is mentioned by
dbSNPrs1816002
ebirs1816002
HLIrs1816002
Exacrs1816002
Varsomers1816002
Maprs1816002
PheGenIrs1816002
hapmaprs1816002
1000 genomesrs1816002
hgdprs1816002
ensemblrs1816002
gopubmedrs1816002
geneviewrs1816002
scholarrs1816002
googlers1816002
pharmgkbrs1816002
gwascentralrs1816002
openSNPrs1816002
23andMers1816002
23andMe allrs1816002
SNP Nexus

SNPshotrs1816002
SNPdbers1816002
MSV3drs1816002
GWAS Ctlgrs1816002
GMAF0.4559
Max Magnitude
? (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 0.000008
Odds Ratio 2.08 [NR] kg increase


GET Evidence
rs1816002
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.563492
summary