Have questions? Visit https://www.reddit.com/r/SNPedia

rs397509312

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;T) 6 BRCA1 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs397509312(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094794
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509312
ClinGenrs397509312
ebirs397509312
HLIrs397509312
Exacrs397509312
Varsomers397509312
Maprs397509312
PheGenIrs397509312
hapmaprs397509312
1000 genomesrs397509312
hgdprs397509312
ensemblrs397509312
gopubmedrs397509312
geneviewrs397509312
scholarrs397509312
googlers397509312
pharmgkbrs397509312
gwascentralrs397509312
openSNPrs397509312
23andMers397509312
23andMe allrs397509312
SNP Nexus

SNPshotrs397509312
SNPdbers397509312
MSV3drs397509312
GWAS Ctlgrs397509312
Max Magnitude6

BRCA1, c.737delT (p.Leu246Terfs)

ClinVar
Risk rs397509312(-;-)
Alt rs397509312(-;-)
Reference Rs397509312(T;T)
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.41246811delA
CLNSRC ClinVar
CLNACC RCV000049114.3, RCV000241020.1,