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rs10774474

From SNPedia

Orientationplus
Stabilizedplus
Make rs10774474(A;A)
Make rs10774474(A;T)
Make rs10774474(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position951120
GeneRAD52
is asnp
is mentioned by
dbSNPrs10774474
ebirs10774474
HLIrs10774474
Exacrs10774474
Varsomers10774474
Maprs10774474
PheGenIrs10774474
hapmaprs10774474
1000 genomesrs10774474
hgdprs10774474
ensemblrs10774474
gopubmedrs10774474
geneviewrs10774474
scholarrs10774474
googlers10774474
pharmgkbrs10774474
gwascentralrs10774474
openSNPrs10774474
23andMers10774474
23andMe allrs10774474
SNP Nexus

SNPshotrs10774474
SNPdbers10774474
MSV3drs10774474
GWAS Ctlgrs10774474
GMAF0.2994
Max Magnitude

[PMID 23209746OA-icon.png] RAD52 Variants Predict Platinum Resistance and Prognosis of Cervical Cancer

[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. [PMID 27531263] [Genetic variation in DNA repair gene RAD52 is associated with the response to platinum-based chemotherapy in SCLC patients].