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rs6489769

From SNPedia

Orientationplus
Stabilizedplus
Make rs6489769(C;C)
Make rs6489769(C;T)
Make rs6489769(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position963799
GeneRAD52
is asnp
is mentioned by
dbSNPrs6489769
ebirs6489769
HLIrs6489769
Exacrs6489769
Varsomers6489769
Maprs6489769
PheGenIrs6489769
hapmaprs6489769
1000 genomesrs6489769
hgdprs6489769
ensemblrs6489769
gopubmedrs6489769
geneviewrs6489769
scholarrs6489769
googlers6489769
pharmgkbrs6489769
gwascentralrs6489769
openSNPrs6489769
23andMers6489769
23andMe allrs6489769
SNP Nexus

SNPshotrs6489769
SNPdbers6489769
MSV3drs6489769
GWAS Ctlgrs6489769
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25012956] A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chinese


[PMID 26629180OA-icon.png] Identification of an SCLC susceptibility rs7963551 genetic polymorphism in a previously GWAS-identified 12p13.33 RAD52 lung cancer risk locus in the Chinese population.