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rs878853577

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853577(-;-)
Make rs878853577(-;CATC)
Make rs878853577(CATC;CATC)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338362
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853577
ebirs878853577
HLIrs878853577
Exacrs878853577
Varsomers878853577
Maprs878853577
PheGenIrs878853577
hapmaprs878853577
1000 genomesrs878853577
hgdprs878853577
ensemblrs878853577
gopubmedrs878853577
geneviewrs878853577
scholarrs878853577
googlers878853577
pharmgkbrs878853577
gwascentralrs878853577
openSNPrs878853577
23andMers878853577
23andMe allrs878853577
SNP Nexus

SNPshotrs878853577
SNPdbers878853577
MSV3drs878853577
GWAS Ctlgrs878853577
Max Magnitude0
ClinVar
Risk rs878853577(CATC;CATC)
Alt rs878853577(CATC;CATC)
Reference rs878853577(;)
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.32912499_32912500insCATC
CLNSRC
CLNACC RCV000226629.1,