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rs863224469

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224469(A;T)
Make rs863224469(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32363345
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224469
ebirs863224469
HLIrs863224469
Exacrs863224469
Varsomers863224469
Maprs863224469
PheGenIrs863224469
hapmaprs863224469
1000 genomesrs863224469
hgdprs863224469
ensemblrs863224469
gopubmedrs863224469
geneviewrs863224469
scholarrs863224469
googlers863224469
pharmgkbrs863224469
gwascentralrs863224469
openSNPrs863224469
23andMers863224469
23andMe allrs863224469
SNP Nexus

SNPshotrs863224469
SNPdbers863224469
MSV3drs863224469
GWAS Ctlgrs863224469
Max Magnitude0
ClinVar
Risk rs863224469(T;T)
Alt rs863224469(T;T)
Reference rs863224469(A;A)
Significance Pathogenic
Disease Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32937482A>T
CLNSRC
CLNACC RCV000199997.1, RCV000221489.1, RCV000238968.1,