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rs568027879

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs568027879(A;A)
Make rs568027879(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position32329440
GeneBRCA2
is asnp
is mentioned by
dbSNPrs568027879
ebirs568027879
HLIrs568027879
Exacrs568027879
Varsomers568027879
Maprs568027879
PheGenIrs568027879
hapmaprs568027879
1000 genomesrs568027879
hgdprs568027879
ensemblrs568027879
gopubmedrs568027879
geneviewrs568027879
scholarrs568027879
googlers568027879
pharmgkbrs568027879
gwascentralrs568027879
openSNPrs568027879
23andMers568027879
23andMe allrs568027879
SNP Nexus

SNPshotrs568027879
SNPdbers568027879
MSV3drs568027879
GWAS Ctlgrs568027879
Max Magnitude0
ClinVar
Risk rs568027879(A,G;A,G)
Alt rs568027879(A,G;A,G)
Reference rs568027879(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Tumor susceptibility linked to germline BAP1 mutations Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32903577C>A; NC_000013.10:g.32903577C>G
CLNSRC
CLNACC RCV000165268.1, RCV000204368.1, RCV000220060.1, RCV000238832.1,