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rs7732671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs7732671(C;C)
Make rs7732671(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position149832680
GenePPARGC1B
is asnp
is mentioned by
dbSNPrs7732671
ebirs7732671
HLIrs7732671
Exacrs7732671
Varsomers7732671
Maprs7732671
PheGenIrs7732671
hapmaprs7732671
1000 genomesrs7732671
hgdprs7732671
ensemblrs7732671
gopubmedrs7732671
geneviewrs7732671
scholarrs7732671
googlers7732671
pharmgkbrs7732671
gwascentralrs7732671
openSNPrs7732671
23andMers7732671
23andMe allrs7732671
SNP Nexus

SNPshotrs7732671
SNPdbers7732671
MSV3drs7732671
GWAS Ctlgrs7732671
GMAF0.1028
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM608886
DescOBESITY, VARIATION IN
Variant0001
Relatedalso


ClinVar
Risk rs7732671(C;C)
Alt rs7732671(C;C)
Reference rs7732671(G;G)
Significance Other
Disease Obesity
Variation info
Gene PPARGC1B
CLNDBN Obesity, variation in
Reversed 0
HGVS NC_000005.9:g.149212243G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002119.3,



[PMID 19166596OA-icon.png] Circadian polymorphisms associated with affective disorders.


GET Evidence
PPARGC1B-A203P
aa_change Ala203Pro
aa_change_short A203P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.109779
summary