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rs2491132

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2491132(C;T)
Make rs2491132(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position30876800
GeneSDC3
is asnp
is mentioned by
dbSNPrs2491132
ebirs2491132
HLIrs2491132
Exacrs2491132
Varsomers2491132
Maprs2491132
PheGenIrs2491132
hapmaprs2491132
1000 genomesrs2491132
hgdprs2491132
ensemblrs2491132
gopubmedrs2491132
geneviewrs2491132
scholarrs2491132
googlers2491132
pharmgkbrs2491132
gwascentralrs2491132
openSNPrs2491132
23andMers2491132
23andMe allrs2491132
SNP Nexus

SNPshotrs2491132
SNPdbers2491132
MSV3drs2491132
GWAS Ctlgrs2491132
GMAF0.101
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM186357
DescSYNDECAN 3; SDC3
Variant
Relatedalso
OMIM186357
Desc
Variant0002
Relatedalso


ClinVar
Risk rs2491132(G,T;G,T)
Alt rs2491132(G,T;G,T)
Reference rs2491132(C;C)
Significance Other
Disease Obesity
Variation info
Gene SDC3
CLNDBN Obesity, association with
Reversed 0
HGVS NC_000001.10:g.31349647C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013593.17,



[PMID 14606043OA-icon.png] Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35.


[PMID 17018662] Positive association of obesity with single nucleotide polymorphisms of syndecan 3 in the Korean population.


GET Evidence
SDC3-V208I
aa_change Val208Ile
aa_change_short V208I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.151264
summary