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rs9966412

From SNPedia

Orientationplus
Stabilizedplus
Make rs9966412(C;C)
Make rs9966412(C;T)
Make rs9966412(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position60366702
is asnp
is mentioned by
dbSNPrs9966412
ebirs9966412
HLIrs9966412
Exacrs9966412
Varsomers9966412
Maprs9966412
PheGenIrs9966412
hapmaprs9966412
1000 genomesrs9966412
hgdprs9966412
ensemblrs9966412
gopubmedrs9966412
geneviewrs9966412
scholarrs9966412
googlers9966412
pharmgkbrs9966412
gwascentralrs9966412
openSNPrs9966412
23andMers9966412
23andMe allrs9966412
SNP Nexus

SNPshotrs9966412
SNPdbers9966412
MSV3drs9966412
GWAS Ctlgrs9966412
GMAF0.2264
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23512951OA-icon.png] Variation at the melanocortin 4 receptor gene and response to weight-loss interventions in the diabetes prevention program