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

rs80357074

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357074(C;C)
Make rs80357074(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43057075
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357074
ebirs80357074
HLIrs80357074
Exacrs80357074
Varsomers80357074
Maprs80357074
PheGenIrs80357074
hapmaprs80357074
1000 genomesrs80357074
hgdprs80357074
ensemblrs80357074
gopubmedrs80357074
geneviewrs80357074
scholarrs80357074
googlers80357074
pharmgkbrs80357074
gwascentralrs80357074
openSNPrs80357074
23andMers80357074
23andMe allrs80357074
SNP Nexus

SNPshotrs80357074
SNPdbers80357074
MSV3drs80357074
GWAS Ctlgrs80357074
Max Magnitude0
ClinVar
Risk rs80357074(A,C;A,C)
Alt rs80357074(A,C;A,C)
Reference rs80357074(G;G)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41209092C>G; NC_000017.10:g.41209092C>T
CLNSRC ClinVar
CLNACC RCV000048885.2, RCV000112581.1, RCV000083065.2,