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

rs397509152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs397509152(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082533
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509152
dbSNP (old)rs397509152
ClinGenrs397509152
ebirs397509152
HLIrs397509152
Exacrs397509152
Gnomadrs397509152
Varsomers397509152
Maprs397509152
PheGenIrs397509152
Biobankrs397509152
1000 genomesrs397509152
hgdprs397509152
ensemblrs397509152
gopubmedrs397509152
geneviewrs397509152
scholarrs397509152
googlers397509152
pharmgkbrs397509152
gwascentralrs397509152
openSNPrs397509152
23andMers397509152
23andMe allrs397509152
SNP Nexus

SNPshotrs397509152
SNPdbers397509152
MSV3drs397509152
GWAS Ctlgrs397509152
Max Magnitude6
ClinVar
Risk rs397509152(T;T)
Alt rs397509152(T;T)
Reference Rs397509152(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.41234550C>A
CLNSRC ClinVar
CLNACC RCV000048493.2, RCV000257277.2,