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rs397509337

From SNPedia

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


Make rs397509337(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094604
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509337
dbSNP (old)rs397509337
ClinGenrs397509337
ebirs397509337
HLIrs397509337
Exacrs397509337
Gnomadrs397509337
Varsomers397509337
Maprs397509337
PheGenIrs397509337
Biobankrs397509337
1000 genomesrs397509337
hgdprs397509337
ensemblrs397509337
gopubmedrs397509337
geneviewrs397509337
scholarrs397509337
googlers397509337
pharmgkbrs397509337
gwascentralrs397509337
openSNPrs397509337
23andMers397509337
23andMe allrs397509337
SNP Nexus

SNPshotrs397509337
SNPdbers397509337
MSV3drs397509337
GWAS Ctlgrs397509337
Max Magnitude6
ClinVar
Risk rs397509337(-;-)
Alt rs397509337(-;-)
Reference Rs397509337(A;A)
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.41246621delT
CLNSRC ClinVar
CLNACC RCV000049192.2, RCV000256934.2,