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rs869320797

From SNPedia

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


Make rs869320797(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32356567
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869320797
dbSNP (old)rs869320797
ClinGenrs869320797
ebirs869320797
HLIrs869320797
Exacrs869320797
Gnomadrs869320797
Varsomers869320797
Maprs869320797
PheGenIrs869320797
Biobankrs869320797
1000 genomesrs869320797
hgdprs869320797
ensemblrs869320797
gopubmedrs869320797
geneviewrs869320797
scholarrs869320797
googlers869320797
pharmgkbrs869320797
gwascentralrs869320797
openSNPrs869320797
23andMers869320797
23andMe allrs869320797
SNP Nexus

SNPshotrs869320797
SNPdbers869320797
MSV3drs869320797
GWAS Ctlgrs869320797
Max Magnitude6
ClinVar
Risk rs869320797(-;-)
Alt rs869320797(-;-)
Reference Rs869320797(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32930704delA
CLNSRC
CLNACC RCV000211007.2,