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rs869320799

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869320799(-;-)
Make rs869320799(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32379492
GeneBRCA2
is asnp
is mentioned by
dbSNPrs869320799
ebirs869320799
HLIrs869320799
Exacrs869320799
Varsomers869320799
Maprs869320799
PheGenIrs869320799
hapmaprs869320799
1000 genomesrs869320799
hgdprs869320799
ensemblrs869320799
gopubmedrs869320799
geneviewrs869320799
scholarrs869320799
googlers869320799
pharmgkbrs869320799
gwascentralrs869320799
openSNPrs869320799
23andMers869320799
23andMe allrs869320799
SNP Nexus

SNPshotrs869320799
SNPdbers869320799
MSV3drs869320799
GWAS Ctlgrs869320799
Max Magnitude0
ClinVar
Risk rs869320799(;)
Alt rs869320799(;)
Reference rs869320799(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32953629delA
CLNSRC
CLNACC RCV000211026.1, RCV000239309.1,