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rs11571378

From SNPedia

Orientationminus
Stabilizedminus
Make rs11571378(A;A)
Make rs11571378(A;T)
Make rs11571378(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position950115
GeneRAD52
is asnp
is mentioned by
dbSNPrs11571378
ebirs11571378
HLIrs11571378
Exacrs11571378
Varsomers11571378
Maprs11571378
PheGenIrs11571378
hapmaprs11571378
1000 genomesrs11571378
hgdprs11571378
ensemblrs11571378
gopubmedrs11571378
geneviewrs11571378
scholarrs11571378
googlers11571378
pharmgkbrs11571378
gwascentralrs11571378
openSNPrs11571378
23andMers11571378
23andMe allrs11571378
SNP Nexus

SNPshotrs11571378
SNPdbers11571378
MSV3drs11571378
GWAS Ctlgrs11571378
Max Magnitude

[PMID 25012956] A RAD52 genetic variant located in a miRNA binding site is associated with glioma risk in Han Chinese [PMID 26629180] Identification of an SCLC susceptibility rs7963551 genetic polymorphism in a previously GWAS-identified 12p13.33 RAD52 lung cancer risk locus in the Chinese population.