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rs8046994

From SNPedia

Orientationplus
Stabilizedplus
Make rs8046994(C;C)
Make rs8046994(C;T)
Make rs8046994(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position52610012
is asnp
is mentioned by
dbSNPrs8046994
ebirs8046994
HLIrs8046994
Exacrs8046994
Varsomers8046994
Maprs8046994
PheGenIrs8046994
hapmaprs8046994
1000 genomesrs8046994
hgdprs8046994
ensemblrs8046994
gopubmedrs8046994
geneviewrs8046994
scholarrs8046994
googlers8046994
pharmgkbrs8046994
gwascentralrs8046994
openSNPrs8046994
23andMers8046994
23andMe allrs8046994
SNP Nexus

SNPshotrs8046994
SNPdbers8046994
MSV3drs8046994
GWAS Ctlgrs8046994
GMAF0.4201
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20406955OA-icon.png] Polymorphisms in the TOX3/LOC643714 Locus and Risk of Breast Cancer in African-American Women