Have questions? Visit https://www.reddit.com/r/SNPedia

rs28936407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs28936407(A;A)
Make rs28936407(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position12416831
GenePPARG
is asnp
is mentioned by
dbSNPrs28936407
ebirs28936407
HLIrs28936407
Exacrs28936407
Varsomers28936407
Maprs28936407
PheGenIrs28936407
hapmaprs28936407
1000 genomesrs28936407
hgdprs28936407
ensemblrs28936407
gopubmedrs28936407
geneviewrs28936407
scholarrs28936407
googlers28936407
pharmgkbrs28936407
gwascentralrs28936407
openSNPrs28936407
23andMers28936407
23andMe allrs28936407
SNP Nexus

SNPshotrs28936407
SNPdbers28936407
MSV3drs28936407
GWAS Ctlgrs28936407
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM601487
DescCOLON CANCER, SOMATIC
Variant0006
Relatedalso


ClinVar
Risk rs28936407(A;A)
Alt rs28936407(A;A)
Reference rs28936407(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene PPARG
CLNDBN Carcinoma of colon
Reversed 0
HGVS NC_000003.11:g.12458330G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008611.4,