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rs397507824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;GT) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507824(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340388
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507824
dbSNP (old)rs397507824
ClinGenrs397507824
ebirs397507824
HLIrs397507824
Exacrs397507824
Gnomadrs397507824
Varsomers397507824
Maprs397507824
PheGenIrs397507824
Biobankrs397507824
1000 genomesrs397507824
hgdprs397507824
ensemblrs397507824
gopubmedrs397507824
geneviewrs397507824
scholarrs397507824
googlers397507824
pharmgkbrs397507824
gwascentralrs397507824
openSNPrs397507824
23andMers397507824
23andMe allrs397507824
SNP Nexus

SNPshotrs397507824
SNPdbers397507824
MSV3drs397507824
GWAS Ctlgrs397507824
Max Magnitude6
ClinVar
Risk rs397507824(TG;TG)
Alt rs397507824(TG;TG)
Reference Rs397507824(-;-)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914525_32914526insGT
CLNSRC ClinVar
CLNACC RCV000044825.2, RCV000257839.2,