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rs397509310

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509310(-;-)
Make rs397509310(-;TGTC)
Make rs397509310(TGTC;TGTC)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124023
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs397509310
ebirs397509310
HLIrs397509310
Exacrs397509310
Varsomers397509310
Maprs397509310
PheGenIrs397509310
hapmaprs397509310
1000 genomesrs397509310
hgdprs397509310
ensemblrs397509310
gopubmedrs397509310
geneviewrs397509310
scholarrs397509310
googlers397509310
pharmgkbrs397509310
gwascentralrs397509310
openSNPrs397509310
23andMers397509310
23andMe allrs397509310
SNP Nexus

SNPshotrs397509310
SNPdbers397509310
MSV3drs397509310
GWAS Ctlgrs397509310
Max Magnitude0
ClinVar
Risk rs397509310(TGTC;TGTC)
Alt rs397509310(TGTC;TGTC)
Reference rs397509310(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41276041_41276044dupGACA
CLNSRC ClinVar
CLNACC RCV000049105.2,