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rs10849605

From SNPedia

Orientationplus
Stabilizedplus
Make rs10849605(C;C)
Make rs10849605(C;T)
Make rs10849605(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position955272
GeneRAD52
is asnp
is mentioned by
dbSNPrs10849605
ebirs10849605
HLIrs10849605
Exacrs10849605
Varsomers10849605
Maprs10849605
PheGenIrs10849605
hapmaprs10849605
1000 genomesrs10849605
hgdprs10849605
ensemblrs10849605
gopubmedrs10849605
geneviewrs10849605
scholarrs10849605
googlers10849605
pharmgkbrs10849605
gwascentralrs10849605
openSNPrs10849605
23andMers10849605
23andMe allrs10849605
SNP Nexus

SNPshotrs10849605
SNPdbers10849605
MSV3drs10849605
GWAS Ctlgrs10849605
GMAF0.4486
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22899653OA-icon.png]
Trait Lung cancer
Title Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
Risk Allele
P-val 6E-7
Odds Ratio 1.08 [1.04-1.11]


[PMID 20805886OA-icon.png] Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID.


[PMID 25793373OA-icon.png] The 12p13.33/RAD52 Locus and Genetic Susceptibility to Squamous Cell Cancers of Upper Aerodigestive Tract


[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.