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rs397507385

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507385(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32355111
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507385
dbSNP (old)rs397507385
ClinGenrs397507385
ebirs397507385
HLIrs397507385
Exacrs397507385
Gnomadrs397507385
Varsomers397507385
Maprs397507385
PheGenIrs397507385
Biobankrs397507385
1000 genomesrs397507385
hgdprs397507385
ensemblrs397507385
gopubmedrs397507385
geneviewrs397507385
scholarrs397507385
googlers397507385
pharmgkbrs397507385
gwascentralrs397507385
openSNPrs397507385
23andMers397507385
23andMe allrs397507385
SNP Nexus

SNPshotrs397507385
SNPdbers397507385
MSV3drs397507385
GWAS Ctlgrs397507385
Max Magnitude6
ClinVar
Risk rs397507385(T;T)
Alt rs397507385(T;T)
Reference Rs397507385(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32929248G>T
CLNSRC ClinVar
CLNACC RCV000031671.5, RCV000045178.3, RCV000221529.1,