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rs397507791

From SNPedia

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


Make rs397507791(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339947
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507791
ClinGenrs397507791
ebirs397507791
HLIrs397507791
Exacrs397507791
Varsomers397507791
Maprs397507791
PheGenIrs397507791
hapmaprs397507791
1000 genomesrs397507791
hgdprs397507791
ensemblrs397507791
gopubmedrs397507791
geneviewrs397507791
scholarrs397507791
googlers397507791
pharmgkbrs397507791
gwascentralrs397507791
openSNPrs397507791
23andMers397507791
23andMe allrs397507791
SNP Nexus

SNPshotrs397507791
SNPdbers397507791
MSV3drs397507791
GWAS Ctlgrs397507791
Max Magnitude6
ClinVar
Risk rs397507791(-;-)
Alt rs397507791(-;-)
Reference Rs397507791(AC;AC)
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.32914084_32914085delCA
CLNSRC ClinVar
CLNACC RCV000044689.2, RCV000257382.2,