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rs3734353

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3734353(A;C)
Make rs3734353(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position100448693
GeneSIM1
is asnp
is mentioned by
dbSNPrs3734353
dbSNP (old)rs3734353
ClinGenrs3734353
ebirs3734353
HLIrs3734353
Exacrs3734353
Gnomadrs3734353
Varsomers3734353
Maprs3734353
PheGenIrs3734353
Biobankrs3734353
1000 genomesrs3734353
hgdprs3734353
ensemblrs3734353
gopubmedrs3734353
geneviewrs3734353
scholarrs3734353
googlers3734353
pharmgkbrs3734353
gwascentralrs3734353
openSNPrs3734353
23andMers3734353
23andMe allrs3734353
SNP Nexus

SNPshotrs3734353
SNPdbers3734353
MSV3drs3734353
GWAS Ctlgrs3734353
GMAF0.3517
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 21512513OA-icon.png] Replication and extension of association between common genetic variants in SIM1 and human adiposity


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


ClinVar
Risk rs3734353(C;C)
Alt rs3734353(C;C)
Reference Rs3734353(A;A)
Significance Non-pathogenic
Disease Schaaf-yang syndrome
Variation info
Gene SIM1
CLNDBN Schaaf-yang syndrome
Reversed 1
HGVS NC_000006.11:g.100896569T>G
CLNSRC
CLNACC RCV000358187.1,