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rs7474896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs7474896(C;T)
Make rs7474896(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position37693169
is asnp
is mentioned by
dbSNPrs7474896
ebirs7474896
HLIrs7474896
Exacrs7474896
Varsomers7474896
Maprs7474896
PheGenIrs7474896
hapmaprs7474896
1000 genomesrs7474896
hgdprs7474896
ensemblrs7474896
gopubmedrs7474896
geneviewrs7474896
scholarrs7474896
googlers7474896
pharmgkbrs7474896
gwascentralrs7474896
openSNPrs7474896
23andMers7474896
23andMe allrs7474896
SNP Nexus

SNPshotrs7474896
SNPdbers7474896
MSV3drs7474896
GWAS Ctlgrs7474896
GMAF0.1047
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele T
P-val 9E-7
Odds Ratio 1.46 [1.25-1.69]


GET Evidence
rs7474896
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary