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rs2660852

From SNPedia

Orientationplus
Stabilizedplus
Make rs2660852(A;A)
Make rs2660852(A;C)
Make rs2660852(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position96051770
is asnp
is mentioned by
dbSNPrs2660852
dbSNP (classic)rs2660852
ClinGenrs2660852
ebirs2660852
HLIrs2660852
Exacrs2660852
Gnomadrs2660852
Varsomers2660852
LitVarrs2660852
Maprs2660852
PheGenIrs2660852
Biobankrs2660852
1000 genomesrs2660852
hgdprs2660852
ensemblrs2660852
geneviewrs2660852
scholarrs2660852
googlers2660852
pharmgkbrs2660852
gwascentralrs2660852
openSNPrs2660852
23andMers2660852
SNPshotrs2660852
SNPdbers2660852
MSV3drs2660852
GWAS Ctlgrs2660852
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 26959888OA-icon.png] Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.