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rs374748

From SNPedia

Orientationplus
Stabilizedplus
Make rs374748(A;A)
Make rs374748(A;G)
Make rs374748(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position128363682
GeneFBN2
is asnp
is mentioned by
dbSNPrs374748
ClinGenrs374748
ebirs374748
HLIrs374748
Exacrs374748
Varsomers374748
Maprs374748
PheGenIrs374748
hapmaprs374748
1000 genomesrs374748
hgdprs374748
ensemblrs374748
gopubmedrs374748
geneviewrs374748
scholarrs374748
googlers374748
pharmgkbrs374748
gwascentralrs374748
openSNPrs374748
23andMers374748
23andMe allrs374748
SNP Nexus

SNPshotrs374748
SNPdbers374748
MSV3drs374748
GWAS Ctlgrs374748
GMAF0.1276
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19553259OA-icon.png]
Trait Obesity (extreme)
Title Common BMI-associated variants confer risk of extreme obesity
Risk Allele G
P-val 0.000004
Odds Ratio 1.47 [1.25-1.73]


GET Evidence
rs374748
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.879032
summary