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rs878853573

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853573(-;-)
Make rs878853573(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338043
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853573
ebirs878853573
HLIrs878853573
Exacrs878853573
Varsomers878853573
Maprs878853573
PheGenIrs878853573
hapmaprs878853573
1000 genomesrs878853573
hgdprs878853573
ensemblrs878853573
gopubmedrs878853573
geneviewrs878853573
scholarrs878853573
googlers878853573
pharmgkbrs878853573
gwascentralrs878853573
openSNPrs878853573
23andMers878853573
23andMe allrs878853573
SNP Nexus

SNPshotrs878853573
SNPdbers878853573
MSV3drs878853573
GWAS Ctlgrs878853573
Max Magnitude0
ClinVar
Risk rs878853573(;)
Alt rs878853573(;)
Reference rs878853573(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.32912180delT
CLNSRC
CLNACC RCV000231965.1,