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rs7963551

From SNPedia

Orientationplus
Stabilizedplus
Make rs7963551(G;G)
Make rs7963551(G;T)
Make rs7963551(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position912349
GeneRAD52
is asnp
is mentioned by
dbSNPrs7963551
ebirs7963551
HLIrs7963551
Exacrs7963551
Varsomers7963551
Maprs7963551
PheGenIrs7963551
hapmaprs7963551
1000 genomesrs7963551
hgdprs7963551
ensemblrs7963551
gopubmedrs7963551
geneviewrs7963551
scholarrs7963551
googlers7963551
pharmgkbrs7963551
gwascentralrs7963551
openSNPrs7963551
23andMers7963551
23andMe allrs7963551
SNP Nexus

SNPshotrs7963551
SNPdbers7963551
MSV3drs7963551
GWAS Ctlgrs7963551
GMAF0.1299
Max Magnitude

[PMID 23188672] Genetic variation in a hsa-let-7 binding site in RAD52 is associated with breast cancer susceptibility

[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.