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rs869320798

From SNPedia

Orientationplus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs869320798(C;C)
Make rs869320798(C;GA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32371034
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869320798
ebirs869320798
HLIrs869320798
Exacrs869320798
Varsomers869320798
Maprs869320798
PheGenIrs869320798
hapmaprs869320798
1000 genomesrs869320798
hgdprs869320798
ensemblrs869320798
gopubmedrs869320798
geneviewrs869320798
scholarrs869320798
googlers869320798
pharmgkbrs869320798
gwascentralrs869320798
openSNPrs869320798
23andMers869320798
23andMe allrs869320798
SNP Nexus

SNPshotrs869320798
SNPdbers869320798
MSV3drs869320798
GWAS Ctlgrs869320798
Max Magnitude0
ClinVar
Risk rs869320798(C;C)
Alt rs869320798(C;C)
Reference rs869320798(GA;GA)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32945171_32945172delGAinsC
CLNSRC
CLNACC RCV000210990.1,