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rs13265018

From SNPedia

Orientationplus
Stabilizedplus
Make rs13265018(A;A)
Make rs13265018(A;G)
Make rs13265018(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position23028507
GeneTNFRSF10B
is asnp
is mentioned by
dbSNPrs13265018
ebirs13265018
HLIrs13265018
Exacrs13265018
Varsomers13265018
Maprs13265018
PheGenIrs13265018
hapmaprs13265018
1000 genomesrs13265018
hgdprs13265018
ensemblrs13265018
gopubmedrs13265018
geneviewrs13265018
scholarrs13265018
googlers13265018
pharmgkbrs13265018
gwascentralrs13265018
openSNPrs13265018
23andMers13265018
23andMe allrs13265018
SNP Nexus

SNPshotrs13265018
SNPdbers13265018
MSV3drs13265018
GWAS Ctlgrs13265018
GMAF0.1226
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene TNFRSF10B
allele G
frequency 0.893
sift TOLERATED
HuRef 1103652271759
Disease Association Defects in TNFRSF10B may be a cause of squamous cell carcinoma of the head and neck (HNSCC) (MIM:275355).



GET Evidence
TNFRSF10B-V191A
aa_change Val191Ala
aa_change_short V191A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.852947
summary