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

rs34585297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs34585297(G;T)
Make rs34585297(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position138584825
GeneTRIM24
is asnp
is mentioned by
dbSNPrs34585297
ebirs34585297
HLIrs34585297
Exacrs34585297
Varsomers34585297
Maprs34585297
PheGenIrs34585297
hapmaprs34585297
1000 genomesrs34585297
hgdprs34585297
ensemblrs34585297
gopubmedrs34585297
geneviewrs34585297
scholarrs34585297
googlers34585297
pharmgkbrs34585297
gwascentralrs34585297
openSNPrs34585297
23andMers34585297
23andMe allrs34585297
SNP Nexus

SNPshotrs34585297
SNPdbers34585297
MSV3drs34585297
GWAS Ctlgrs34585297
Max Magnitude0
Venter snp
Source plos
Gene TRIM24
allele T
frequency
sift AFFECT FUNCTION
HuRef 1103652718176
Disease Association A chromosomal aberration involving TIF1 is a cause of thyroid papillary carcinoma (PACT) (MIM:188550). Translocation t(7;10)(q32;q11) with RET. The translocation generates the TIF1/RET (PTC6) oncogene.



GET Evidence
TRIM24-R975S
aa_change Arg975Ser
aa_change_short R975S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency
summary