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rs863224468

From SNPedia

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


Make rs863224468(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32362589
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224468
dbSNP (old)rs863224468
ClinGenrs863224468
ebirs863224468
HLIrs863224468
Exacrs863224468
Gnomadrs863224468
Varsomers863224468
Maprs863224468
PheGenIrs863224468
Biobankrs863224468
1000 genomesrs863224468
hgdprs863224468
ensemblrs863224468
gopubmedrs863224468
geneviewrs863224468
scholarrs863224468
googlers863224468
pharmgkbrs863224468
gwascentralrs863224468
openSNPrs863224468
23andMers863224468
23andMe allrs863224468
SNP Nexus

SNPshotrs863224468
SNPdbers863224468
MSV3drs863224468
GWAS Ctlgrs863224468
Max Magnitude6
ClinVar
Risk rs863224468(C;C) rs863224468(G;G)
Alt rs863224468(C;C) rs863224468(G;G)
Reference Rs863224468(T;T)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32936726T>C; NC_000013.10:g.32936726T>G
CLNSRC
CLNACC RCV000233488.1, RCV000200163.1, RCV000241341.1,