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rs1129424

From SNPedia

Orientationminus
Stabilizedminus
Make rs1129424(C;C)
Make rs1129424(C;T)
Make rs1129424(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position23068800
GenePOU3F4, TNFRSF10B
is asnp
is mentioned by
dbSNPrs1129424
ebirs1129424
HLIrs1129424
Exacrs1129424
Varsomers1129424
Maprs1129424
PheGenIrs1129424
hapmaprs1129424
1000 genomesrs1129424
hgdprs1129424
ensemblrs1129424
gopubmedrs1129424
geneviewrs1129424
scholarrs1129424
googlers1129424
pharmgkbrs1129424
gwascentralrs1129424
openSNPrs1129424
23andMers1129424
23andMe allrs1129424
SNP Nexus

SNPshotrs1129424
SNPdbers1129424
MSV3drs1129424
GWAS Ctlgrs1129424
GMAF0.2567
Max Magnitude
? (C;C) (C;T) (T;T) 28


Venter snp
Source plos
Gene TNFRSF10B
allele A
frequency
sift TOLERATED
HuRef 1103652271861
Disease Association Defects in TNFRSF10B may be a cause of squamous cell carcinoma of the head and neck (HNSCC) (MIM:275355).



GET Evidence
TNFRSF10B-P32L
aa_change Pro32Leu
aa_change_short P32L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.653128
summary