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rs397509303

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509303(-;-)
Make rs397509303(-;T)
Make rs397509303(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124034
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs397509303
ebirs397509303
HLIrs397509303
Exacrs397509303
Varsomers397509303
Maprs397509303
PheGenIrs397509303
hapmaprs397509303
1000 genomesrs397509303
hgdprs397509303
ensemblrs397509303
gopubmedrs397509303
geneviewrs397509303
scholarrs397509303
googlers397509303
pharmgkbrs397509303
gwascentralrs397509303
openSNPrs397509303
23andMers397509303
23andMe allrs397509303
SNP Nexus

SNPshotrs397509303
SNPdbers397509303
MSV3drs397509303
GWAS Ctlgrs397509303
Max Magnitude0
ClinVar
Risk rs397509303(T;T)
Alt rs397509303(T;T)
Reference rs397509303(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41276052dupA
CLNSRC ClinVar
CLNACC RCV000049075.2,