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rs80359190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;T) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs80359190(A;G)
Make rs80359190(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380136
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359190
dbSNP (old)rs80359190
ClinGenrs80359190
ebirs80359190
HLIrs80359190
Exacrs80359190
Gnomadrs80359190
Varsomers80359190
Maprs80359190
PheGenIrs80359190
Biobankrs80359190
1000 genomesrs80359190
hgdprs80359190
ensemblrs80359190
gopubmedrs80359190
geneviewrs80359190
scholarrs80359190
googlers80359190
pharmgkbrs80359190
gwascentralrs80359190
openSNPrs80359190
23andMers80359190
23andMe allrs80359190
SNP Nexus

SNPshotrs80359190
SNPdbers80359190
MSV3drs80359190
GWAS Ctlgrs80359190
Max Magnitude6
ClinVar
Risk rs80359190(G;G) rs80359190(T;T)
Alt rs80359190(G;G) rs80359190(T;T)
Reference Rs80359190(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32954273A>G; NC_000013.10:g.32954273A>T
CLNSRC ClinVar
CLNACC RCV000031806.4, RCV000045756.5, RCV000212286.2, RCV000221707.1, RCV000045757.2, RCV000256545.2,