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rs397507757

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;A) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs397507757(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339441
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507757
dbSNP (old)rs397507757
ClinGenrs397507757
ebirs397507757
HLIrs397507757
Exacrs397507757
Gnomadrs397507757
Varsomers397507757
Maprs397507757
PheGenIrs397507757
Biobankrs397507757
1000 genomesrs397507757
hgdprs397507757
ensemblrs397507757
gopubmedrs397507757
geneviewrs397507757
scholarrs397507757
googlers397507757
pharmgkbrs397507757
gwascentralrs397507757
openSNPrs397507757
23andMers397507757
23andMe allrs397507757
SNP Nexus

SNPshotrs397507757
SNPdbers397507757
MSV3drs397507757
GWAS Ctlgrs397507757
Max Magnitude6
ClinVar
Risk rs397507757(A;A)
Alt rs397507757(A;A)
Reference Rs397507757(-;-)
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.32913578_32913579insA
CLNSRC ClinVar
CLNACC RCV000044551.2, RCV000257431.2,