rs7732671

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs7732671(C;C)

Make rs7732671(C;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

149832680

Gene

PPARGC1B

is a	snp
is	mentioned by
dbSNP	rs7732671
dbSNP (classic)	rs7732671
ClinGen	rs7732671
ebi	rs7732671
HLI	rs7732671
Exac	rs7732671
Gnomad	rs7732671
Varsome	rs7732671
LitVar	rs7732671
Map	rs7732671
PheGenI	rs7732671
Biobank	rs7732671
1000 genomes	rs7732671
hgdp	rs7732671
ensembl	rs7732671
geneview	rs7732671
scholar	rs7732671
google	rs7732671
pharmgkb	rs7732671
gwascentral	rs7732671
openSNP	rs7732671
23andMe	rs7732671
SNPshot	rs7732671
SNPdbe	rs7732671
MSV3d	rs7732671
GWAS Ctlg	rs7732671

GMAF

0.1028

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

OMIM	608886
Desc	OBESITY, VARIATION IN
Variant	0001
Related	also

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 UniProtKB (protein)
CLNACC	RCV000002119.3,

[PMID 19166596] Circadian polymorphisms associated with affective disorders.