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rs863224828

From SNPedia

Orientationplus
Make rs863224828(-;-)
Make rs863224828(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position32362663
GeneBRCA2
is asnp
is mentioned by
dbSNPrs863224828
ebirs863224828
HLIrs863224828
Exacrs863224828
Varsomers863224828
Maprs863224828
PheGenIrs863224828
hapmaprs863224828
1000 genomesrs863224828
hgdprs863224828
ensemblrs863224828
gopubmedrs863224828
geneviewrs863224828
scholarrs863224828
googlers863224828
pharmgkbrs863224828
gwascentralrs863224828
openSNPrs863224828
23andMers863224828
23andMe allrs863224828
SNP Nexus

SNPshotrs863224828
SNPdbers863224828
MSV3drs863224828
GWAS Ctlgrs863224828
Max Magnitude
ClinVar
Risk rs863224828(;)
Alt rs863224828(;)
Reference rs863224828(C;C)
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.32936800delC
CLNSRC
CLNACC RCV000196534.1,