Have questions? Visit https://www.reddit.com/r/SNPedia

rs80356880

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356880(C;G)
Make rs80356880(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115750
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356880
ebirs80356880
HLIrs80356880
Exacrs80356880
Varsomers80356880
Maprs80356880
PheGenIrs80356880
hapmaprs80356880
1000 genomesrs80356880
hgdprs80356880
ensemblrs80356880
gopubmedrs80356880
geneviewrs80356880
scholarrs80356880
googlers80356880
pharmgkbrs80356880
gwascentralrs80356880
openSNPrs80356880
23andMers80356880
23andMe allrs80356880
SNP Nexus

SNPshotrs80356880
SNPdbers80356880
MSV3drs80356880
GWAS Ctlgrs80356880
Max Magnitude0
ClinVar
Risk rs80356880(A,G;A,G)
Alt rs80356880(A,G;A,G)
Reference rs80356880(C;C)
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.41267767G>C; NC_000017.10:g.41267767G>T
CLNSRC Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified by a quantitative integrated evaluation
CLNACC RCV000047345.2, RCV000077482.3, RCV000164121.1, RCV000047344.2, RCV000111781.2,