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rs80358099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358099(G;T)
Make rs80358099(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051118
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358099
ebirs80358099
HLIrs80358099
Exacrs80358099
Varsomers80358099
Maprs80358099
PheGenIrs80358099
hapmaprs80358099
1000 genomesrs80358099
hgdprs80358099
ensemblrs80358099
gopubmedrs80358099
geneviewrs80358099
scholarrs80358099
googlers80358099
pharmgkbrs80358099
gwascentralrs80358099
openSNPrs80358099
23andMers80358099
23andMe allrs80358099
SNP Nexus

SNPshotrs80358099
SNPdbers80358099
MSV3drs80358099
GWAS Ctlgrs80358099
Max Magnitude0
ClinVar
Risk rs80358099(A,C,T;A,C,T)
Alt rs80358099(A,C,T;A,C,T)
Reference rs80358099(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 not provided Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41203135C>A; NC_000017.10:g.41203135C>G; NC_000017.10:g.41203135C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048905.4, RCV000112598.1, RCV000212198.1, RCV000048904.2, RCV000077612.2, RCV000129416.2, RCV000048903.2, RCV000112597.1,