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rs863224467

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224467(A;T)
Make rs863224467(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32340377
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224467
ebirs863224467
HLIrs863224467
Exacrs863224467
Varsomers863224467
Maprs863224467
PheGenIrs863224467
hapmaprs863224467
1000 genomesrs863224467
hgdprs863224467
ensemblrs863224467
gopubmedrs863224467
geneviewrs863224467
scholarrs863224467
googlers863224467
pharmgkbrs863224467
gwascentralrs863224467
openSNPrs863224467
23andMers863224467
23andMe allrs863224467
SNP Nexus

SNPshotrs863224467
SNPdbers863224467
MSV3drs863224467
GWAS Ctlgrs863224467
Max Magnitude0
ClinVar
Risk rs863224467(T;T)
Alt rs863224467(T;T)
Reference rs863224467(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32914514A>T
CLNSRC
CLNACC RCV000195698.1,