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rs397509332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397509332(G;G)
Make rs397509332(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124089
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs397509332
ebirs397509332
HLIrs397509332
Exacrs397509332
Varsomers397509332
Maprs397509332
PheGenIrs397509332
hapmaprs397509332
1000 genomesrs397509332
hgdprs397509332
ensemblrs397509332
gopubmedrs397509332
geneviewrs397509332
scholarrs397509332
googlers397509332
pharmgkbrs397509332
gwascentralrs397509332
openSNPrs397509332
23andMers397509332
23andMe allrs397509332
SNP Nexus

SNPshotrs397509332
SNPdbers397509332
MSV3drs397509332
GWAS Ctlgrs397509332
Max Magnitude0
ClinVar
Risk rs397509332(C,G;C,G)
Alt rs397509332(C,G;C,G)
Reference rs397509332(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41276106A>C
CLNSRC ClinVar
CLNACC RCV000049181.2,