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rs878853599

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853599(-;-)
Make rs878853599(-;T)
Make rs878853599(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32355000
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853599
ebirs878853599
HLIrs878853599
Exacrs878853599
Varsomers878853599
Maprs878853599
PheGenIrs878853599
hapmaprs878853599
1000 genomesrs878853599
hgdprs878853599
ensemblrs878853599
gopubmedrs878853599
geneviewrs878853599
scholarrs878853599
googlers878853599
pharmgkbrs878853599
gwascentralrs878853599
openSNPrs878853599
23andMers878853599
23andMe allrs878853599
SNP Nexus

SNPshotrs878853599
SNPdbers878853599
MSV3drs878853599
GWAS Ctlgrs878853599
Max Magnitude0
ClinVar
Risk rs878853599(T;T)
Alt rs878853599(T;T)
Reference rs878853599(;)
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.32929137dupT
CLNSRC
CLNACC RCV000227767.1,