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rs121909246

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909246(C;T)
Make rs121909246(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12392713
GenePPARG
is asnp
is mentioned by
dbSNPrs121909246
ebirs121909246
HLIrs121909246
Exacrs121909246
Varsomers121909246
Maprs121909246
PheGenIrs121909246
hapmaprs121909246
1000 genomesrs121909246
hgdprs121909246
ensemblrs121909246
gopubmedrs121909246
geneviewrs121909246
scholarrs121909246
googlers121909246
pharmgkbrs121909246
gwascentralrs121909246
openSNPrs121909246
23andMers121909246
23andMe allrs121909246
SNP Nexus

SNPshotrs121909246
SNPdbers121909246
MSV3drs121909246
GWAS Ctlgrs121909246
Max Magnitude0
OMIM601487
Desc
Variant0015
Relatedalso
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,