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rs80356905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80356905(C;C)
Make rs80356905(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43051113
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356905
ebirs80356905
HLIrs80356905
Exacrs80356905
Varsomers80356905
Maprs80356905
PheGenIrs80356905
hapmaprs80356905
1000 genomesrs80356905
hgdprs80356905
ensemblrs80356905
gopubmedrs80356905
geneviewrs80356905
scholarrs80356905
googlers80356905
pharmgkbrs80356905
gwascentralrs80356905
openSNPrs80356905
23andMers80356905
23andMe allrs80356905
SNP Nexus

SNPshotrs80356905
SNPdbers80356905
MSV3drs80356905
GWAS Ctlgrs80356905
Max Magnitude0
ClinVar
Risk rs80356905(C;C)
Alt rs80356905(C;C)
Reference rs80356905(T;T)
Significance Untested
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.41203130A>G
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000048908.2, RCV000112600.1, RCV000131349.2,