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rs397509083

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs397509083(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091952
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509083
dbSNP (old)rs397509083
ClinGenrs397509083
ebirs397509083
HLIrs397509083
Exacrs397509083
Gnomadrs397509083
Varsomers397509083
Maprs397509083
PheGenIrs397509083
Biobankrs397509083
1000 genomesrs397509083
hgdprs397509083
ensemblrs397509083
gopubmedrs397509083
geneviewrs397509083
scholarrs397509083
googlers397509083
pharmgkbrs397509083
gwascentralrs397509083
openSNPrs397509083
23andMers397509083
23andMe allrs397509083
SNP Nexus

SNPshotrs397509083
SNPdbers397509083
MSV3drs397509083
GWAS Ctlgrs397509083
Max Magnitude6
ClinVar
Risk rs397509083(T;T)
Alt rs397509083(T;T)
Reference Rs397509083(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41243970dupA
CLNSRC ClinVar
CLNACC RCV000048236.2, RCV000257563.2,