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rs80358004

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358004(A;A)
Make rs80358004(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063332
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358004
ebirs80358004
HLIrs80358004
Exacrs80358004
Varsomers80358004
Maprs80358004
PheGenIrs80358004
hapmaprs80358004
1000 genomesrs80358004
hgdprs80358004
ensemblrs80358004
gopubmedrs80358004
geneviewrs80358004
scholarrs80358004
googlers80358004
pharmgkbrs80358004
gwascentralrs80358004
openSNPrs80358004
23andMers80358004
23andMe allrs80358004
SNP Nexus

SNPshotrs80358004
SNPdbers80358004
MSV3drs80358004
GWAS Ctlgrs80358004
Max Magnitude0
ClinVar
Risk rs80358004(A,C,T;A,C,T)
Alt rs80358004(A,C,T;A,C,T)
Reference rs80358004(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41215349C>A; NC_000017.10:g.41215349C>G; NC_000017.10:g.41215349C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000077159.2, RCV000160001.2, RCV000048848.2, RCV000112550.1, RCV000131171.2, RCV000083063.3,