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

rs397509288

From SNPedia

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


Make rs397509288(-;-)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045787
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509288
dbSNP (old)rs397509288
ClinGenrs397509288
ebirs397509288
HLIrs397509288
Exacrs397509288
Varsomers397509288
Maprs397509288
PheGenIrs397509288
Biobankrs397509288
1000 genomesrs397509288
hgdprs397509288
ensemblrs397509288
gopubmedrs397509288
geneviewrs397509288
scholarrs397509288
googlers397509288
pharmgkbrs397509288
gwascentralrs397509288
openSNPrs397509288
23andMers397509288
23andMe allrs397509288
SNP Nexus

SNPshotrs397509288
SNPdbers397509288
MSV3drs397509288
GWAS Ctlgrs397509288
Max Magnitude6
ClinVar
Risk rs397509288(-;-)
Alt rs397509288(-;-)
Reference Rs397509288(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.41197804delC
CLNSRC ClinVar
CLNACC RCV000049012.2, RCV000257522.2,