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rs1973993

From SNPedia

Orientationplus
Stabilizedplus
Make rs1973993(C;C)
Make rs1973993(C;T)
Make rs1973993(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position96478438
is asnp
is mentioned by
dbSNPrs1973993
dbSNP (classic)rs1973993
ClinGenrs1973993
ebirs1973993
HLIrs1973993
Exacrs1973993
Gnomadrs1973993
Varsomers1973993
LitVarrs1973993
Maprs1973993
PheGenIrs1973993
Biobankrs1973993
1000 genomesrs1973993
hgdprs1973993
ensemblrs1973993
geneviewrs1973993
scholarrs1973993
googlers1973993
pharmgkbrs1973993
gwascentralrs1973993
openSNPrs1973993
23andMers1973993
SNPshotrs1973993
SNPdbers1973993
MSV3drs1973993
GWAS Ctlgrs1973993
GMAF0.438
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 19079260]
Trait Weight
Title Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Risk Allele C
P-val 0.000001
Odds Ratio 2.71 [1.61-3.81] % SD