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rs80357492

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357492(C;C)
Make rs80357492(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43082541
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357492
ebirs80357492
HLIrs80357492
Exacrs80357492
Varsomers80357492
Maprs80357492
PheGenIrs80357492
hapmaprs80357492
1000 genomesrs80357492
hgdprs80357492
ensemblrs80357492
gopubmedrs80357492
geneviewrs80357492
scholarrs80357492
googlers80357492
pharmgkbrs80357492
gwascentralrs80357492
openSNPrs80357492
23andMers80357492
23andMe allrs80357492
SNP Nexus

SNPshotrs80357492
SNPdbers80357492
MSV3drs80357492
GWAS Ctlgrs80357492
Max Magnitude0
ClinVar
Risk rs80357492(A,C;A,C)
Alt rs80357492(A,C;A,C)
Reference rs80357492(T;T)
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.41234558A>G
CLNSRC ClinVar
CLNACC RCV000048491.2, RCV000112300.1,