rs72551363

Orientation

plus

Stabilized

plus

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

Make rs72551363(A;A)

Make rs72551363(A;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12417048

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs72551363
dbSNP (classic)	rs72551363
ClinGen	rs72551363
ebi	rs72551363
HLI	rs72551363
Exac	rs72551363
Gnomad	rs72551363
Varsome	rs72551363
LitVar	rs72551363
Map	rs72551363
PheGenI	rs72551363
Biobank	rs72551363
1000 genomes	rs72551363
hgdp	rs72551363
ensembl	rs72551363
geneview	rs72551363
scholar	rs72551363
google	rs72551363
pharmgkb	rs72551363
gwascentral	rs72551363
openSNP	rs72551363
23andMe	rs72551363
SNPshot	rs72551363
SNPdbe	rs72551363
MSV3d	rs72551363
GWAS Ctlg	rs72551363

Max Magnitude

0

OMIM	601487
Desc
Variant	0012
Related	also

ClinVar
Risk	rs72551363(A;A)
Alt	rs72551363(A;A)
Reference	Rs72551363(T;T)
Significance	Pathogenic
Disease	Familial partial lipodystrophy 3
Variation	info
Gene	PPARG
CLNDBN	Familial partial lipodystrophy 3
Reversed	0
HGVS	NC_000003.11:g.12458547T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008618.3,