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rs80357475

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357475(G;T)
Make rs80357475(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124094
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs80357475
ebirs80357475
HLIrs80357475
Exacrs80357475
Varsomers80357475
Maprs80357475
PheGenIrs80357475
hapmaprs80357475
1000 genomesrs80357475
hgdprs80357475
ensemblrs80357475
gopubmedrs80357475
geneviewrs80357475
scholarrs80357475
googlers80357475
pharmgkbrs80357475
gwascentralrs80357475
openSNPrs80357475
23andMers80357475
23andMe allrs80357475
SNP Nexus

SNPshotrs80357475
SNPdbers80357475
MSV3drs80357475
GWAS Ctlgrs80357475
Max Magnitude0
ClinVar
Risk rs80357475(T;T)
Alt rs80357475(T;T)
Reference rs80357475(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene NBR2 BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41276111C>A
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000048405.3, RCV000111552.1, RCV000131890.2,