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rs1060878

From SNPedia

Orientationplus
Stabilizedplus
Make rs1060878(A;A)
Make rs1060878(A;G)
Make rs1060878(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position39348941
GeneCTAGE5
is asnp
is mentioned by
dbSNPrs1060878
ebirs1060878
HLIrs1060878
Exacrs1060878
Varsomers1060878
Maprs1060878
PheGenIrs1060878
hapmaprs1060878
1000 genomesrs1060878
hgdprs1060878
ensemblrs1060878
gopubmedrs1060878
geneviewrs1060878
scholarrs1060878
googlers1060878
pharmgkbrs1060878
gwascentralrs1060878
openSNPrs1060878
23andMers1060878
23andMe allrs1060878
SNP Nexus

SNPshotrs1060878
SNPdbers1060878
MSV3drs1060878
GWAS Ctlgrs1060878
GMAF0.2938
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene CTAGE5
allele A
frequency
sift TOLERATED
HuRef 1103649039393
Disease Association Autoantigen found several cancer, including benign meningioma and cutaneous T-cell lymphoma (CTCL). Isoform 5A and isoform 5B are recognized by patients'sera with tumor specimen of various origins.



Neighborrs1140952
Distance117


GET Evidence
CTAGE5-G738R
aa_change Gly738Arg
aa_change_short G738R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.350381
summary