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rs863224464

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224464(A;G)
Make rs863224464(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32316461
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224464
ebirs863224464
HLIrs863224464
Exacrs863224464
Varsomers863224464
Maprs863224464
PheGenIrs863224464
hapmaprs863224464
1000 genomesrs863224464
hgdprs863224464
ensemblrs863224464
gopubmedrs863224464
geneviewrs863224464
scholarrs863224464
googlers863224464
pharmgkbrs863224464
gwascentralrs863224464
openSNPrs863224464
23andMers863224464
23andMe allrs863224464
SNP Nexus

SNPshotrs863224464
SNPdbers863224464
MSV3drs863224464
GWAS Ctlgrs863224464
Max Magnitude0
ClinVar
Risk rs863224464(G;G)
Alt rs863224464(G;G)
Reference rs863224464(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.32890598A>G
CLNSRC
CLNACC RCV000195819.1,