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rs397507703

From SNPedia

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


Make rs397507703(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338450
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507703
dbSNP (old)rs397507703
ClinGenrs397507703
ebirs397507703
HLIrs397507703
Exacrs397507703
Varsomers397507703
Maprs397507703
PheGenIrs397507703
Biobankrs397507703
1000 genomesrs397507703
hgdprs397507703
ensemblrs397507703
gopubmedrs397507703
geneviewrs397507703
scholarrs397507703
googlers397507703
pharmgkbrs397507703
gwascentralrs397507703
openSNPrs397507703
23andMers397507703
23andMe allrs397507703
SNP Nexus

SNPshotrs397507703
SNPdbers397507703
MSV3drs397507703
GWAS Ctlgrs397507703
Max Magnitude6
ClinVar
Risk rs397507703(-;-)
Alt rs397507703(-;-)
Reference Rs397507703(T;T)
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.32912587delT
CLNSRC ClinVar
CLNACC RCV000044348.2, RCV000257085.2,