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rs80357001

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80357001(C;T)
Make rs80357001(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094839
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357001
ebirs80357001
HLIrs80357001
Exacrs80357001
Varsomers80357001
Maprs80357001
PheGenIrs80357001
hapmaprs80357001
1000 genomesrs80357001
hgdprs80357001
ensemblrs80357001
gopubmedrs80357001
geneviewrs80357001
scholarrs80357001
googlers80357001
pharmgkbrs80357001
gwascentralrs80357001
openSNPrs80357001
23andMers80357001
23andMe allrs80357001
SNP Nexus

SNPshotrs80357001
SNPdbers80357001
MSV3drs80357001
GWAS Ctlgrs80357001
Max Magnitude0
ClinVar
Risk rs80357001(T;T)
Alt rs80357001(T;T)
Reference rs80357001(C;C)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not specified
Reversed 1
HGVS NC_000017.10:g.41246856G>A
CLNSRC ClinVar
CLNACC RCV000049098.4, RCV000112772.1, RCV000162837.1, RCV000235122.1,