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rs397507836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;CA) 6 BRCA2 variant considered pathogenic for breast cancer
(CA;CA) 0 common in clinvar


Make rs397507836(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340623
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507836
dbSNP (old)rs397507836
ClinGenrs397507836
ebirs397507836
HLIrs397507836
Exacrs397507836
Gnomadrs397507836
Varsomers397507836
Maprs397507836
PheGenIrs397507836
Biobankrs397507836
1000 genomesrs397507836
hgdprs397507836
ensemblrs397507836
gopubmedrs397507836
geneviewrs397507836
scholarrs397507836
googlers397507836
pharmgkbrs397507836
gwascentralrs397507836
openSNPrs397507836
23andMers397507836
23andMe allrs397507836
SNP Nexus

SNPshotrs397507836
SNPdbers397507836
MSV3drs397507836
GWAS Ctlgrs397507836
Max Magnitude6
ClinVar
Risk rs397507836(-;-)
Alt rs397507836(-;-)
Reference Rs397507836(CA;CA)
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.32914760_32914761delCA
CLNSRC ClinVar
CLNACC RCV000044882.2, RCV000256957.2,