rs121909245

Orientation

plus

Stabilized

plus

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

Make rs121909245(A;A)

Make rs121909245(A;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12392701

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs121909245
dbSNP (classic)	rs121909245
ClinGen	rs121909245
ebi	rs121909245
HLI	rs121909245
Exac	rs121909245
Gnomad	rs121909245
Varsome	rs121909245
LitVar	rs121909245
Map	rs121909245
PheGenI	rs121909245
Biobank	rs121909245
1000 genomes	rs121909245
hgdp	rs121909245
ensembl	rs121909245
geneview	rs121909245
scholar	rs121909245
google	rs121909245
pharmgkb	rs121909245
gwascentral	rs121909245
openSNP	rs121909245
23andMe	rs121909245
SNPshot	rs121909245
SNPdbe	rs121909245
MSV3d	rs121909245
GWAS Ctlg	rs121909245

Max Magnitude

0

OMIM	601487
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121909245(A;A)
Alt	rs121909245(A;A)
Reference	Rs121909245(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.12434200T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008620.2,