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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
ebirs1973993
HLIrs1973993
Exacrs1973993
Varsomers1973993
Maprs1973993
PheGenIrs1973993
hapmaprs1973993
1000 genomesrs1973993
hgdprs1973993
ensemblrs1973993
gopubmedrs1973993
geneviewrs1973993
scholarrs1973993
googlers1973993
pharmgkbrs1973993
gwascentralrs1973993
openSNPrs1973993
23andMers1973993
23andMe allrs1973993
SNP Nexus

SNPshotrs1973993
SNPdbers1973993
MSV3drs1973993
GWAS Ctlgrs1973993
GMAF0.438
Max Magnitude
? (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



GET Evidence
rs1973993
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.445312
summary