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rs6842544

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6842544(C;C)
Make rs6842544(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position152411407
GeneFBXW7
is asnp
is mentioned by
dbSNPrs6842544
ebirs6842544
HLIrs6842544
Exacrs6842544
Varsomers6842544
Maprs6842544
PheGenIrs6842544
hapmaprs6842544
1000 genomesrs6842544
hgdprs6842544
ensemblrs6842544
gopubmedrs6842544
geneviewrs6842544
scholarrs6842544
googlers6842544
pharmgkbrs6842544
gwascentralrs6842544
openSNPrs6842544
23andMers6842544
23andMe allrs6842544
SNP Nexus

SNPshotrs6842544
SNPdbers6842544
MSV3drs6842544
GWAS Ctlgrs6842544
GMAF0.002755
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 22348067OA-icon.png] Allele-Specific Deletions in Mouse Tumors Identify Fbxw7 as Germline Modifier of Tumor Susceptibility


ClinVar
Risk rs6842544(C;C)
Alt rs6842544(C;C)
Reference rs6842544(T;T)
Significance Untested
Disease not specified
Variation info
Gene FBXW7
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.153332559T>C
CLNSRC ClinVar
CLNACC RCV000121056.1,