rs72551362

Orientation

plus

Stabilized

plus

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

Make rs72551362(A;A)

Make rs72551362(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12416836

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs72551362
dbSNP (classic)	rs72551362
ClinGen	rs72551362
ebi	rs72551362
HLI	rs72551362
Exac	rs72551362
Gnomad	rs72551362
Varsome	rs72551362
LitVar	rs72551362
Map	rs72551362
PheGenI	rs72551362
Biobank	rs72551362
1000 genomes	rs72551362
hgdp	rs72551362
ensembl	rs72551362
geneview	rs72551362
scholar	rs72551362
google	rs72551362
pharmgkb	rs72551362
gwascentral	rs72551362
openSNP	rs72551362
23andMe	rs72551362
SNPshot	rs72551362
SNPdbe	rs72551362
MSV3d	rs72551362
GWAS Ctlg	rs72551362

Max Magnitude

0

OMIM	601487
Desc
Variant	0008
Related	also

ClinVar
Risk	rs72551362(A;A)
Alt	rs72551362(A;A)
Reference	Rs72551362(G;G)
Significance	Pathogenic
Disease	Familial partial lipodystrophy 3
Variation	info
Gene	PPARG
CLNDBN	Familial partial lipodystrophy 3
Reversed	0
HGVS	NC_000003.11:g.12458335G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008613.4,