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rs878853299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTG;CTG) 0 common in clinvar
(CTG;TT) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs878853299(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32338746
GeneBRCA2
is asnp
is mentioned by
dbSNPrs878853299
dbSNP (old)rs878853299
ClinGenrs878853299
ebirs878853299
HLIrs878853299
Exacrs878853299
Gnomadrs878853299
Varsomers878853299
Maprs878853299
PheGenIrs878853299
Biobankrs878853299
1000 genomesrs878853299
hgdprs878853299
ensemblrs878853299
gopubmedrs878853299
geneviewrs878853299
scholarrs878853299
googlers878853299
pharmgkbrs878853299
gwascentralrs878853299
openSNPrs878853299
23andMers878853299
23andMe allrs878853299
SNP Nexus

SNPshotrs878853299
SNPdbers878853299
MSV3drs878853299
GWAS Ctlgrs878853299
Max Magnitude6
ClinVar
Risk rs878853299(TT;TT)
Alt rs878853299(TT;TT)
Reference Rs878853299(CTG;CTG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32912883_32912885delCTGinsTT
CLNSRC
CLNACC RCV000225602.1,