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rs397507961

From SNPedia

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


Make rs397507961(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363266
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507961
dbSNP (old)rs397507961
ClinGenrs397507961
ebirs397507961
HLIrs397507961
Exacrs397507961
Varsomers397507961
Maprs397507961
PheGenIrs397507961
Biobankrs397507961
1000 genomesrs397507961
hgdprs397507961
ensemblrs397507961
gopubmedrs397507961
geneviewrs397507961
scholarrs397507961
googlers397507961
pharmgkbrs397507961
gwascentralrs397507961
openSNPrs397507961
23andMers397507961
23andMe allrs397507961
SNP Nexus

SNPshotrs397507961
SNPdbers397507961
MSV3drs397507961
GWAS Ctlgrs397507961
Max Magnitude6
ClinVar
Risk rs397507961(-;-)
Alt rs397507961(-;-)
Reference Rs397507961(TC;TC)
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.32937403_32937404delCT
CLNSRC ClinVar
CLNACC RCV000045409.2, RCV000256904.2,