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rs878853611

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs878853611(-;-)
Make rs878853611(-;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32371053
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853611
ebirs878853611
HLIrs878853611
Exacrs878853611
Varsomers878853611
Maprs878853611
PheGenIrs878853611
hapmaprs878853611
1000 genomesrs878853611
hgdprs878853611
ensemblrs878853611
gopubmedrs878853611
geneviewrs878853611
scholarrs878853611
googlers878853611
pharmgkbrs878853611
gwascentralrs878853611
openSNPrs878853611
23andMers878853611
23andMe allrs878853611
SNP Nexus

SNPshotrs878853611
SNPdbers878853611
MSV3drs878853611
GWAS Ctlgrs878853611
Max Magnitude0
ClinVar
Risk rs878853611(;)
Alt rs878853611(;)
Reference rs878853611(TA;TA)
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.32945190_32945191delTA
CLNSRC
CLNACC RCV000230336.1,