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

rs6593669

From SNPedia

Orientationplus
Stabilizedplus
Make rs6593669(C;C)
Make rs6593669(C;T)
Make rs6593669(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position95568926
is asnp
is mentioned by
dbSNPrs6593669
dbSNP (old)rs6593669
ClinGenrs6593669
ebirs6593669
HLIrs6593669
Exacrs6593669
Gnomadrs6593669
Varsomers6593669
Maprs6593669
PheGenIrs6593669
Biobankrs6593669
1000 genomesrs6593669
hgdprs6593669
ensemblrs6593669
gopubmedrs6593669
geneviewrs6593669
scholarrs6593669
googlers6593669
pharmgkbrs6593669
gwascentralrs6593669
openSNPrs6593669
23andMers6593669
23andMe allrs6593669
SNP Nexus

SNPshotrs6593669
SNPdbers6593669
MSV3drs6593669
GWAS Ctlgrs6593669
GMAF0.331
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20054173] Genotype-phenotype associations in obesity dependent on definition of the obesity phenotype