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rs878853560

From SNPedia

Orientationplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs878853560(-;-)
Make rs878853560(-;TG)
Make rs878853560(TG;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32336506
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853560
ebirs878853560
HLIrs878853560
Exacrs878853560
Varsomers878853560
Maprs878853560
PheGenIrs878853560
hapmaprs878853560
1000 genomesrs878853560
hgdprs878853560
ensemblrs878853560
gopubmedrs878853560
geneviewrs878853560
scholarrs878853560
googlers878853560
pharmgkbrs878853560
gwascentralrs878853560
openSNPrs878853560
23andMers878853560
23andMe allrs878853560
SNP Nexus

SNPshotrs878853560
SNPdbers878853560
MSV3drs878853560
GWAS Ctlgrs878853560
Max Magnitude0
ClinVar
Risk rs878853560(;)
Alt rs878853560(;)
Reference rs878853560(GT;GT)
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.32910643_32910644delTG
CLNSRC
CLNACC RCV000226260.1,