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

rs3734354

From SNPedia

Orientationminus
Stabilizedminus
Make rs3734354(A;A)
Make rs3734354(A;C)
Make rs3734354(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position100420903
GeneLOC102724406, SIM1
is asnp
is mentioned by
dbSNPrs3734354
ebirs3734354
HLIrs3734354
Exacrs3734354
Varsomers3734354
Maprs3734354
PheGenIrs3734354
hapmaprs3734354
1000 genomesrs3734354
hgdprs3734354
ensemblrs3734354
gopubmedrs3734354
geneviewrs3734354
scholarrs3734354
googlers3734354
pharmgkbrs3734354
gwascentralrs3734354
openSNPrs3734354
23andMers3734354
23andMe allrs3734354
SNP Nexus

SNPshotrs3734354
SNPdbers3734354
MSV3drs3734354
GWAS Ctlgrs3734354
GMAF0.197
Max Magnitude
? (A;A) (A;C) (C;C) 28
[PMID 20075856OA-icon.png] Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population


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


[PMID 17357083OA-icon.png] Medical sequencing at the extremes of human body mass.


[PMID 19401419OA-icon.png] Common variation in SIM1 is reproducibly associated with BMI in Pima Indians.


[PMID 21671989OA-icon.png] Dosing equation for tacrolimus using genetic variants and clinical factors.


GET Evidence
SIM1-P352T
aa_change Pro352Thr
aa_change_short P352T
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0996468
summary