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rs9390322

From SNPedia

Merged intors2328686
Orientationplus
Stabilizedplus
Make rs9390322(C;C)
Make rs9390322(C;T)
Make rs9390322(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position145443150
is asnp
is mentioned by
dbSNPrs9390322
ebirs9390322
HLIrs9390322
Exacrs9390322
Varsomers9390322
Maprs9390322
PheGenIrs9390322
hapmaprs9390322
1000 genomesrs9390322
hgdprs9390322
ensemblrs9390322
gopubmedrs9390322
geneviewrs9390322
scholarrs9390322
googlers9390322
pharmgkbrs9390322
gwascentralrs9390322
openSNPrs9390322
23andMers9390322
23andMe allrs9390322
SNP Nexus

SNPshotrs9390322
SNPdbers9390322
MSV3drs9390322
GWAS Ctlgrs9390322
StatusMerged into rs2328686
Max Magnitude

[PMID 21512513OA-icon.png] Replication and extension of association between common genetic variants in SIM1 and human adiposity