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rs80359195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359195(A;C)
Make rs80359195(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32394707
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359195
ebirs80359195
HLIrs80359195
Exacrs80359195
Varsomers80359195
Maprs80359195
PheGenIrs80359195
hapmaprs80359195
1000 genomesrs80359195
hgdprs80359195
ensemblrs80359195
gopubmedrs80359195
geneviewrs80359195
scholarrs80359195
googlers80359195
pharmgkbrs80359195
gwascentralrs80359195
openSNPrs80359195
23andMers80359195
23andMe allrs80359195
SNP Nexus

SNPshotrs80359195
SNPdbers80359195
MSV3drs80359195
GWAS Ctlgrs80359195
Max Magnitude0
ClinVar
Risk rs80359195(C,G,T;C,G,T)
Alt rs80359195(C,G,T;C,G,T)
Reference rs80359195(A;A)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32968844A>C; NC_000013.10:g.32968844A>G; NC_000013.10:g.32968844A>T
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000045773.3, RCV000077465.3, RCV000045774.3, RCV000077466.5, RCV000131684.2, RCV000077039.2, RCV000167271.1,