rs121909246

Orientation

plus

Stabilized

plus

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

Make rs121909246(C;T)

Make rs121909246(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12392713

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs121909246
dbSNP (classic)	rs121909246
ClinGen	rs121909246
ebi	rs121909246
HLI	rs121909246
Exac	rs121909246
Gnomad	rs121909246
Varsome	rs121909246
LitVar	rs121909246
Map	rs121909246
PheGenI	rs121909246
Biobank	rs121909246
1000 genomes	rs121909246
hgdp	rs121909246
ensembl	rs121909246
geneview	rs121909246
scholar	rs121909246
google	rs121909246
pharmgkb	rs121909246
gwascentral	rs121909246
openSNP	rs121909246
23andMe	rs121909246
SNPshot	rs121909246
SNPdbe	rs121909246
MSV3d	rs121909246
GWAS Ctlg	rs121909246

Max Magnitude

0

OMIM	601487
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121909246(T;T)
Alt	rs121909246(T;T)
Reference	Rs121909246(C;C)
Significance	Pathogenic
Disease	Familial partial lipodystrophy 3
Variation	info
Gene	PPARG
CLNDBN	Familial partial lipodystrophy 3
Reversed	0
HGVS	NC_000003.11:g.12434212C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008621.2,