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rs80359186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80359186(A;G)
Make rs80359186(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32380107
GeneBRCA2
is asnp
is mentioned by
dbSNPrs80359186
ebirs80359186
HLIrs80359186
Exacrs80359186
Varsomers80359186
Maprs80359186
PheGenIrs80359186
hapmaprs80359186
1000 genomesrs80359186
hgdprs80359186
ensemblrs80359186
gopubmedrs80359186
geneviewrs80359186
scholarrs80359186
googlers80359186
pharmgkbrs80359186
gwascentralrs80359186
openSNPrs80359186
23andMers80359186
23andMe allrs80359186
SNP Nexus

SNPshotrs80359186
SNPdbers80359186
MSV3drs80359186
GWAS Ctlgrs80359186
Max Magnitude0
ClinVar
Risk rs80359186(G;G)
Alt rs80359186(G;G)
Reference rs80359186(A;A)
Significance Untested
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.32954244A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000045750.3, RCV000077464.3, RCV000130237.2,