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rs77275268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs77275268(C;T)
Make rs77275268(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position151648063
is asnp
is mentioned by
dbSNPrs77275268
ebirs77275268
HLIrs77275268
Exacrs77275268
Varsomers77275268
Maprs77275268
PheGenIrs77275268
hapmaprs77275268
1000 genomesrs77275268
hgdprs77275268
ensemblrs77275268
gopubmedrs77275268
geneviewrs77275268
scholarrs77275268
googlers77275268
pharmgkbrs77275268
gwascentralrs77275268
openSNPrs77275268
23andMers77275268
23andMe allrs77275268
SNP Nexus

SNPshotrs77275268
SNPdbers77275268
MSV3drs77275268
GWAS Ctlgrs77275268
GMAF0.1166
Max Magnitude0

[PMID 20661439OA-icon.png] Ancestry-Shift Refinement Mapping of the C6orf97-ESR1 Breast Cancer Susceptibility Locus