Have questions? Visit https://www.reddit.com/r/SNPedia

rs7603514

From SNPedia

Orientationplus
Stabilizedplus
Make rs7603514(A;A)
Make rs7603514(A;G)
Make rs7603514(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position205971888
is asnp
is mentioned by
dbSNPrs7603514
ebirs7603514
HLIrs7603514
Exacrs7603514
Varsomers7603514
Maprs7603514
PheGenIrs7603514
hapmaprs7603514
1000 genomesrs7603514
hgdprs7603514
ensemblrs7603514
gopubmedrs7603514
geneviewrs7603514
scholarrs7603514
googlers7603514
pharmgkbrs7603514
gwascentralrs7603514
openSNPrs7603514
23andMers7603514
23andMe allrs7603514
SNP Nexus

SNPshotrs7603514
SNPdbers7603514
MSV3drs7603514
GWAS Ctlgrs7603514
GMAF0.1864
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 A
P-val 0.000008
Odds Ratio 1.36 [1.19-1.56]


GET Evidence
rs7603514
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary