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rs80359031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359031(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363190
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359031
ClinGenrs80359031
ebirs80359031
HLIrs80359031
Exacrs80359031
Varsomers80359031
Maprs80359031
PheGenIrs80359031
hapmaprs80359031
1000 genomesrs80359031
hgdprs80359031
ensemblrs80359031
gopubmedrs80359031
geneviewrs80359031
scholarrs80359031
googlers80359031
pharmgkbrs80359031
gwascentralrs80359031
openSNPrs80359031
23andMers80359031
23andMe allrs80359031
SNP Nexus

SNPshotrs80359031
SNPdbers80359031
MSV3drs80359031
GWAS Ctlgrs80359031
Max Magnitude6
ClinVar
Risk rs80359031(T;T)
Alt rs80359031(T;T)
Reference Rs80359031(A;A)
Significance Other
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Reversed 0
HGVS NC_000013.10:g.32937327A>T
CLNSRC ClinVar
CLNACC RCV000077422.5, RCV000163034.1, RCV000257984.2, RCV000484277.1,