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rs72551363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72551363(A;A)
Make rs72551363(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12417048
GenePPARG
is asnp
is mentioned by
dbSNPrs72551363
ebirs72551363
HLIrs72551363
Exacrs72551363
Varsomers72551363
Maprs72551363
PheGenIrs72551363
hapmaprs72551363
1000 genomesrs72551363
hgdprs72551363
ensemblrs72551363
gopubmedrs72551363
geneviewrs72551363
scholarrs72551363
googlers72551363
pharmgkbrs72551363
gwascentralrs72551363
openSNPrs72551363
23andMers72551363
23andMe allrs72551363
SNP Nexus

SNPshotrs72551363
SNPdbers72551363
MSV3drs72551363
GWAS Ctlgrs72551363
Max Magnitude0
OMIM601487
Desc
Variant0012
Relatedalso


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 RCV000008618.2,