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rs121909243

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121909243(A;T)
Make rs121909243(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12416923
GenePPARG
is asnp
is mentioned by
dbSNPrs121909243
ebirs121909243
HLIrs121909243
Exacrs121909243
Varsomers121909243
Maprs121909243
PheGenIrs121909243
hapmaprs121909243
1000 genomesrs121909243
hgdprs121909243
ensemblrs121909243
gopubmedrs121909243
geneviewrs121909243
scholarrs121909243
googlers121909243
pharmgkbrs121909243
gwascentralrs121909243
openSNPrs121909243
23andMers121909243
23andMe allrs121909243
SNP Nexus

SNPshotrs121909243
SNPdbers121909243
MSV3drs121909243
GWAS Ctlgrs121909243
Max Magnitude0
OMIM601487
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121909243(T;T)
Alt rs121909243(T;T)
Reference rs121909243(A;A)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene PPARG
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000003.11:g.12458422A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008610.4,