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rs3734355

From SNPedia

Orientationminus
Stabilizedminus
Make rs3734355(C;C)
Make rs3734355(C;T)
Make rs3734355(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position100420845
GeneSIM1
is asnp
is mentioned by
dbSNPrs3734355
ebirs3734355
HLIrs3734355
Exacrs3734355
Varsomers3734355
Maprs3734355
PheGenIrs3734355
hapmaprs3734355
1000 genomesrs3734355
hgdprs3734355
ensemblrs3734355
gopubmedrs3734355
geneviewrs3734355
scholarrs3734355
googlers3734355
pharmgkbrs3734355
gwascentralrs3734355
openSNPrs3734355
23andMers3734355
23andMe allrs3734355
SNP Nexus

SNPshotrs3734355
SNPdbers3734355
MSV3drs3734355
GWAS Ctlgrs3734355
GMAF0.1979
Max Magnitude
? (C;C) (C;T) (T;T) 28
[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.


GET Evidence
SIM1-A371V
aa_change Ala371Val
aa_change_short A371V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0998327
summary