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rs863224825

From SNPedia

Orientationplus
Make rs863224825(-;-)
Make rs863224825(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32338531
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224825
ebirs863224825
HLIrs863224825
Exacrs863224825
Varsomers863224825
Maprs863224825
PheGenIrs863224825
hapmaprs863224825
1000 genomesrs863224825
hgdprs863224825
ensemblrs863224825
gopubmedrs863224825
geneviewrs863224825
scholarrs863224825
googlers863224825
pharmgkbrs863224825
gwascentralrs863224825
openSNPrs863224825
23andMers863224825
23andMe allrs863224825
SNP Nexus

SNPshotrs863224825
SNPdbers863224825
MSV3drs863224825
GWAS Ctlgrs863224825
Max Magnitude
ClinVar
Risk rs863224825(;)
Alt rs863224825(;)
Reference rs863224825(T;T)
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.32912668delT
CLNSRC
CLNACC RCV000195447.1,