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rs121909245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909245(A;A)
Make rs121909245(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12392701
GenePPARG
is asnp
is mentioned by
dbSNPrs121909245
ebirs121909245
HLIrs121909245
Exacrs121909245
Varsomers121909245
Maprs121909245
PheGenIrs121909245
hapmaprs121909245
1000 genomesrs121909245
hgdprs121909245
ensemblrs121909245
gopubmedrs121909245
geneviewrs121909245
scholarrs121909245
googlers121909245
pharmgkbrs121909245
gwascentralrs121909245
openSNPrs121909245
23andMers121909245
23andMe allrs121909245
SNP Nexus

SNPshotrs121909245
SNPdbers121909245
MSV3drs121909245
GWAS Ctlgrs121909245
Max Magnitude0
OMIM601487
Desc
Variant0014
Relatedalso
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,