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rs863224465

From SNPedia
Merged intors80359473
Orientationplus
Stabilizedplus
Geno Mag Summary
(AAAG;AAAG) 0 common in clinvar
Make rs863224465(-;-)
Make rs863224465(-;AAAG)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339288
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224465
dbSNP (old)rs863224465
ClinGenrs863224465
ebirs863224465
HLIrs863224465
Exacrs863224465
Gnomadrs863224465
Varsomers863224465
Maprs863224465
PheGenIrs863224465
Biobankrs863224465
1000 genomesrs863224465
hgdprs863224465
ensemblrs863224465
gopubmedrs863224465
geneviewrs863224465
scholarrs863224465
googlers863224465
pharmgkbrs863224465
gwascentralrs863224465
openSNPrs863224465
23andMers863224465
23andMe allrs863224465
SNP Nexus

SNPshotrs863224465
SNPdbers863224465
MSV3drs863224465
GWAS Ctlgrs863224465
StatusMerged into rs80359473
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863224465(AAAG;AAAG)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32913428_32913431delGAAA
CLNSRC Breast Cancer Information Core (BRCA2)
CLNACC RCV000031516.7, RCV000074531.7, RCV000131071.3, RCV000198074.3,