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rs397508935

From SNPedia

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


Make rs397508935(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093465
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508935
dbSNP (old)rs397508935
ClinGenrs397508935
ebirs397508935
HLIrs397508935
Exacrs397508935
Varsomers397508935
Maprs397508935
PheGenIrs397508935
Biobankrs397508935
1000 genomesrs397508935
hgdprs397508935
ensemblrs397508935
gopubmedrs397508935
geneviewrs397508935
scholarrs397508935
googlers397508935
pharmgkbrs397508935
gwascentralrs397508935
openSNPrs397508935
23andMers397508935
23andMe allrs397508935
SNP Nexus

SNPshotrs397508935
SNPdbers397508935
MSV3drs397508935
GWAS Ctlgrs397508935
Max Magnitude6
ClinVar
Risk rs397508935(-;-)
Alt rs397508935(-;-)
Reference Rs397508935(CAAG;CAAG)
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.41245482_41245485delCTTG
CLNSRC ClinVar
CLNACC RCV000047697.2, RCV000257753.2,