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rs12769288

From SNPedia

Orientationplus
Stabilizedplus
Make rs12769288(C;C)
Make rs12769288(C;T)
Make rs12769288(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position129488086
GeneMGMT
is asnp
is mentioned by
dbSNPrs12769288
dbSNP (classic)rs12769288
ClinGenrs12769288
ebirs12769288
HLIrs12769288
Exacrs12769288
Gnomadrs12769288
Varsomers12769288
LitVarrs12769288
Maprs12769288
PheGenIrs12769288
Biobankrs12769288
1000 genomesrs12769288
hgdprs12769288
ensemblrs12769288
geneviewrs12769288
scholarrs12769288
googlers12769288
pharmgkbrs12769288
gwascentralrs12769288
openSNPrs12769288
23andMers12769288
23andMe allrs12769288
SNPshotrs12769288
SNPdbers12769288
MSV3drs12769288
GWAS Ctlgrs12769288
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 29263185OA-icon.png] Germline variants in DNA repair genes, diagnostic radiation and risk of thyroid cancer.