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rs397509255

From SNPedia

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


Make rs397509255(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051106
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509255
dbSNP (old)rs397509255
ClinGenrs397509255
ebirs397509255
HLIrs397509255
Exacrs397509255
Gnomadrs397509255
Varsomers397509255
Maprs397509255
PheGenIrs397509255
Biobankrs397509255
1000 genomesrs397509255
hgdprs397509255
ensemblrs397509255
gopubmedrs397509255
geneviewrs397509255
scholarrs397509255
googlers397509255
pharmgkbrs397509255
gwascentralrs397509255
openSNPrs397509255
23andMers397509255
23andMe allrs397509255
SNP Nexus

SNPshotrs397509255
SNPdbers397509255
MSV3drs397509255
GWAS Ctlgrs397509255
Max Magnitude6
ClinVar
Risk rs397509255(-;-)
Alt rs397509255(-;-)
Reference Rs397509255(G;G)
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.41203123delC
CLNSRC ClinVar
CLNACC RCV000048911.2, RCV000257468.2,