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rs80357258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80357258(A;G)
Make rs80357258(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045712
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357258
ebirs80357258
HLIrs80357258
Exacrs80357258
Varsomers80357258
Maprs80357258
PheGenIrs80357258
hapmaprs80357258
1000 genomesrs80357258
hgdprs80357258
ensemblrs80357258
gopubmedrs80357258
geneviewrs80357258
scholarrs80357258
googlers80357258
pharmgkbrs80357258
gwascentralrs80357258
openSNPrs80357258
23andMers80357258
23andMe allrs80357258
SNP Nexus

SNPshotrs80357258
SNPdbers80357258
MSV3drs80357258
GWAS Ctlgrs80357258
Max Magnitude0
ClinVar
Risk rs80357258(G;G)
Alt rs80357258(G;G)
Reference rs80357258(A;A)
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.41197729T>C
CLNSRC ClinVar
CLNACC RCV000049049.2, RCV000112703.1,