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rs769416

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs769416(G;T)
Make rs769416(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position89971229
GeneNBN
is asnp
is mentioned by
dbSNPrs769416
ebirs769416
HLIrs769416
Exacrs769416
Varsomers769416
Maprs769416
PheGenIrs769416
hapmaprs769416
1000 genomesrs769416
hgdprs769416
ensemblrs769416
gopubmedrs769416
geneviewrs769416
scholarrs769416
googlers769416
pharmgkbrs769416
gwascentralrs769416
openSNPrs769416
23andMers769416
23andMe allrs769416
SNP Nexus

SNPshotrs769416
SNPdbers769416
MSV3drs769416
GWAS Ctlgrs769416
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 19714462] Genetic variation in genes interacting with BRCA1/2 and risk of breast cancer in the Cypriot population