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rs863224466

From SNPedia

Orientationplus
Make rs863224466(-;-)
Make rs863224466(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32339793
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224466
ebirs863224466
HLIrs863224466
Exacrs863224466
Varsomers863224466
Maprs863224466
PheGenIrs863224466
hapmaprs863224466
1000 genomesrs863224466
hgdprs863224466
ensemblrs863224466
gopubmedrs863224466
geneviewrs863224466
scholarrs863224466
googlers863224466
pharmgkbrs863224466
gwascentralrs863224466
openSNPrs863224466
23andMers863224466
23andMe allrs863224466
SNP Nexus

SNPshotrs863224466
SNPdbers863224466
MSV3drs863224466
GWAS Ctlgrs863224466
Max Magnitude
ClinVar
Risk rs863224466(;)
Alt rs863224466(;)
Reference rs863224466(T;T)
Significance Pathogenic
Disease Familial cancer of breast Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32913931delT
CLNSRC
CLNACC RCV000044661.2, RCV000198909.1,