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rs4712652

From SNPedia

Orientationplus
Stabilizedplus
Make rs4712652(A;A)
Make rs4712652(A;G)
Make rs4712652(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position22078386
GeneCASC15
is asnp
is mentioned by
dbSNPrs4712652
ebirs4712652
HLIrs4712652
Exacrs4712652
Varsomers4712652
Maprs4712652
PheGenIrs4712652
hapmaprs4712652
1000 genomesrs4712652
hgdprs4712652
ensemblrs4712652
gopubmedrs4712652
geneviewrs4712652
scholarrs4712652
googlers4712652
pharmgkbrs4712652
gwascentralrs4712652
openSNPrs4712652
23andMers4712652
23andMe allrs4712652
SNP Nexus

SNPshotrs4712652
SNPdbers4712652
MSV3drs4712652
GWAS Ctlgrs4712652
GMAF0.2897
Max Magnitude
? (A;A) (A;G) (G;G) 28


[PMID 20846890] A common variant near the PRL gene is associated with increased adiposity in males


[PMID 19553259OA-icon.png] Common body mass index-associated variants confer risk of extreme obesity.


[PMID 20127379OA-icon.png] From monogenic to polygenic obesity: recent advances.


[PMID 22430306OA-icon.png] Evaluation of common genetic variants identified by GWAS for early onset and morbid obesity in population-based samples.


GET Evidence
rs4712652
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.59375
summary