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rs587776687

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776687(-;-)
Make rs587776687(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12392689
GenePPARG
is asnp
is mentioned by
dbSNPrs587776687
ebirs587776687
HLIrs587776687
Exacrs587776687
Varsomers587776687
Maprs587776687
PheGenIrs587776687
hapmaprs587776687
1000 genomesrs587776687
hgdprs587776687
ensemblrs587776687
gopubmedrs587776687
geneviewrs587776687
scholarrs587776687
googlers587776687
pharmgkbrs587776687
gwascentralrs587776687
openSNPrs587776687
23andMers587776687
23andMe allrs587776687
SNP Nexus

SNPshotrs587776687
SNPdbers587776687
MSV3drs587776687
GWAS Ctlgrs587776687
Max Magnitude0
ClinVar
Risk rs587776687(;)
Alt rs587776687(;)
Reference rs587776687(A;A)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene PPARG
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000003.11:g.12434188delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008608.4,