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rs1993709

From SNPedia

Orientationminus
Stabilizedminus
Make rs1993709(C;C)
Make rs1993709(C;T)
Make rs1993709(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position72372846
is asnp
is mentioned by
dbSNPrs1993709
ebirs1993709
HLIrs1993709
Exacrs1993709
Varsomers1993709
Maprs1993709
PheGenIrs1993709
hapmaprs1993709
1000 genomesrs1993709
hgdprs1993709
ensemblrs1993709
gopubmedrs1993709
geneviewrs1993709
scholarrs1993709
googlers1993709
pharmgkbrs1993709
gwascentralrs1993709
openSNPrs1993709
23andMers1993709
23andMe allrs1993709
SNP Nexus

SNPshotrs1993709
SNPdbers1993709
MSV3drs1993709
GWAS Ctlgrs1993709
GMAF0.112
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23563609OA-icon.png]
Trait Obesity (early onset extreme)
Title Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Risk Allele G
P-val 5E-13
Odds Ratio 1.38 [1.26-1.50]