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rs17066856

From SNPedia

Orientationplus
Stabilizedplus
Make rs17066856(C;C)
Make rs17066856(C;T)
Make rs17066856(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position60382423
is asnp
is mentioned by
dbSNPrs17066856
ebirs17066856
HLIrs17066856
Exacrs17066856
Varsomers17066856
Maprs17066856
PheGenIrs17066856
hapmaprs17066856
1000 genomesrs17066856
hgdprs17066856
ensemblrs17066856
gopubmedrs17066856
geneviewrs17066856
scholarrs17066856
googlers17066856
pharmgkbrs17066856
gwascentralrs17066856
openSNPrs17066856
23andMers17066856
23andMe allrs17066856
SNP Nexus

SNPshotrs17066856
SNPdbers17066856
MSV3drs17066856
GWAS Ctlgrs17066856
GMAF0.2002
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