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rs80358076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358076(G;T)
Make rs80358076(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43090943
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358076
ebirs80358076
HLIrs80358076
Exacrs80358076
Varsomers80358076
Maprs80358076
PheGenIrs80358076
hapmaprs80358076
1000 genomesrs80358076
hgdprs80358076
ensemblrs80358076
gopubmedrs80358076
geneviewrs80358076
scholarrs80358076
googlers80358076
pharmgkbrs80358076
gwascentralrs80358076
openSNPrs80358076
23andMers80358076
23andMe allrs80358076
SNP Nexus

SNPshotrs80358076
SNPdbers80358076
MSV3drs80358076
GWAS Ctlgrs80358076
Max Magnitude0
ClinVar
Risk rs80358076(A,T;A,T)
Alt rs80358076(A,T;A,T)
Reference rs80358076(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41242960C>A; NC_000017.10:g.41242960C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048474.2, RCV000077566.4, RCV000165984.1,