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rs80359165

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359165(A;C)
Make rs80359165(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32379900
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359165
ebirs80359165
HLIrs80359165
Exacrs80359165
Varsomers80359165
Maprs80359165
PheGenIrs80359165
hapmaprs80359165
1000 genomesrs80359165
hgdprs80359165
ensemblrs80359165
gopubmedrs80359165
geneviewrs80359165
scholarrs80359165
googlers80359165
pharmgkbrs80359165
gwascentralrs80359165
openSNPrs80359165
23andMers80359165
23andMe allrs80359165
SNP Nexus

SNPshotrs80359165
SNPdbers80359165
MSV3drs80359165
GWAS Ctlgrs80359165
Max Magnitude0
ClinVar
Risk rs80359165(C,G;C,G)
Alt rs80359165(C,G;C,G)
Reference rs80359165(A;A)
Significance Other
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000013.10:g.32954037A>C; NC_000013.10:g.32954037A>G; NC_000013.10:g.32954037A>T
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000031794.5, RCV000045717.6, RCV000120368.2, RCV000130861.2, RCV000045718.5, RCV000114048.1, RCV000203635.1, RCV000222955.1, RCV000222210.1,