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rs72551362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72551362(A;A)
Make rs72551362(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12416836
GenePPARG
is asnp
is mentioned by
dbSNPrs72551362
ebirs72551362
HLIrs72551362
Exacrs72551362
Varsomers72551362
Maprs72551362
PheGenIrs72551362
hapmaprs72551362
1000 genomesrs72551362
hgdprs72551362
ensemblrs72551362
gopubmedrs72551362
geneviewrs72551362
scholarrs72551362
googlers72551362
pharmgkbrs72551362
gwascentralrs72551362
openSNPrs72551362
23andMers72551362
23andMe allrs72551362
SNP Nexus

SNPshotrs72551362
SNPdbers72551362
MSV3drs72551362
GWAS Ctlgrs72551362
Max Magnitude0
OMIM601487
Desc
Variant0008
Relatedalso


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 RCV000008613.3,