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rs863224466

From SNPedia

Merged intors397507785
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224466(-;-)
Make rs863224466(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339793
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224466
dbSNP (old)rs863224466
ClinGenrs863224466
ebirs863224466
HLIrs863224466
Exacrs863224466
Gnomadrs863224466
Varsomers863224466
Maprs863224466
PheGenIrs863224466
Biobankrs863224466
1000 genomesrs863224466
hgdprs863224466
ensemblrs863224466
gopubmedrs863224466
geneviewrs863224466
scholarrs863224466
googlers863224466
pharmgkbrs863224466
gwascentralrs863224466
openSNPrs863224466
23andMers863224466
23andMe allrs863224466
SNP Nexus

SNPshotrs863224466
SNPdbers863224466
MSV3drs863224466
GWAS Ctlgrs863224466
StatusMerged into rs397507785
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs863224466(T;T)
Significance Pathogenic
Disease Familial cancer of breast Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913931delT
CLNSRC
CLNACC RCV000044661.2, RCV000198909.1, RCV000241279.1,