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rs121909242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121909242(A;C)
Make rs121909242(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position12416825
GenePPARG
is asnp
is mentioned by
dbSNPrs121909242
ebirs121909242
HLIrs121909242
Exacrs121909242
Varsomers121909242
Maprs121909242
PheGenIrs121909242
hapmaprs121909242
1000 genomesrs121909242
hgdprs121909242
ensemblrs121909242
gopubmedrs121909242
geneviewrs121909242
scholarrs121909242
googlers121909242
pharmgkbrs121909242
gwascentralrs121909242
openSNPrs121909242
23andMers121909242
23andMe allrs121909242
SNP Nexus

SNPshotrs121909242
SNPdbers121909242
MSV3drs121909242
GWAS Ctlgrs121909242
Max Magnitude0
OMIM601487
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909242(C;C)
Alt rs121909242(C;C)
Reference rs121909242(A;A)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene PPARG
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000003.11:g.12458324A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008609.4,