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rs397509304

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397509304(-;-)
Make rs397509304(-;TT)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124032
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs397509304
ebirs397509304
HLIrs397509304
Exacrs397509304
Varsomers397509304
Maprs397509304
PheGenIrs397509304
hapmaprs397509304
1000 genomesrs397509304
hgdprs397509304
ensemblrs397509304
gopubmedrs397509304
geneviewrs397509304
scholarrs397509304
googlers397509304
pharmgkbrs397509304
gwascentralrs397509304
openSNPrs397509304
23andMers397509304
23andMe allrs397509304
SNP Nexus

SNPshotrs397509304
SNPdbers397509304
MSV3drs397509304
GWAS Ctlgrs397509304
Max Magnitude0
ClinVar
Risk rs397509304(;)
Alt rs397509304(;)
Reference rs397509304(TT;TT)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41276049_41276050delAA
CLNSRC ClinVar
CLNACC RCV000049078.2,