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rs879255330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;TCTC) 6 BRCA2 variant considered pathogenic for breast cancer
(TCTC;TCTC) 0 common in clinvar


Make rs879255330(-;-)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32340821
GeneBRCA2
is asnp
is mentioned by
dbSNPrs879255330
dbSNP (old)rs879255330
ClinGenrs879255330
ebirs879255330
HLIrs879255330
Exacrs879255330
Gnomadrs879255330
Varsomers879255330
Maprs879255330
PheGenIrs879255330
Biobankrs879255330
1000 genomesrs879255330
hgdprs879255330
ensemblrs879255330
gopubmedrs879255330
geneviewrs879255330
scholarrs879255330
googlers879255330
pharmgkbrs879255330
gwascentralrs879255330
openSNPrs879255330
23andMers879255330
23andMe allrs879255330
SNP Nexus

SNPshotrs879255330
SNPdbers879255330
MSV3drs879255330
GWAS Ctlgrs879255330
Max Magnitude6
ClinVar
Risk rs879255330(-;-)
Alt rs879255330(-;-)
Reference Rs879255330(TCTC;TCTC)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32914958_32914961delTCTC
CLNSRC
CLNACC RCV000238933.1, RCV000241080.2,