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rs397509335

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGC;AGC) 0 common in clinvar
Make rs397509335(AGC;T)
Make rs397509335(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094607
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509335
ebirs397509335
HLIrs397509335
Exacrs397509335
Varsomers397509335
Maprs397509335
PheGenIrs397509335
hapmaprs397509335
1000 genomesrs397509335
hgdprs397509335
ensemblrs397509335
gopubmedrs397509335
geneviewrs397509335
scholarrs397509335
googlers397509335
pharmgkbrs397509335
gwascentralrs397509335
openSNPrs397509335
23andMers397509335
23andMe allrs397509335
SNP Nexus

SNPshotrs397509335
SNPdbers397509335
MSV3drs397509335
GWAS Ctlgrs397509335
Max Magnitude0
ClinVar
Risk rs397509335(T;T)
Alt rs397509335(T;T)
Reference rs397509335(AGC;AGC)
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.41246624_41246626delGCTinsA
CLNSRC ClinVar
CLNACC RCV000049188.2, RCV000077633.2,