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

rs80358082

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358082(A;T)
Make rs80358082(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position43074328
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358082
ebirs80358082
HLIrs80358082
Exacrs80358082
Varsomers80358082
Maprs80358082
PheGenIrs80358082
hapmaprs80358082
1000 genomesrs80358082
hgdprs80358082
ensemblrs80358082
gopubmedrs80358082
geneviewrs80358082
scholarrs80358082
googlers80358082
pharmgkbrs80358082
gwascentralrs80358082
openSNPrs80358082
23andMers80358082
23andMe allrs80358082
SNP Nexus

SNPshotrs80358082
SNPdbers80358082
MSV3drs80358082
GWAS Ctlgrs80358082
Max Magnitude0
ClinVar
Risk rs80358082(G,T;G,T)
Alt rs80358082(G,T;G,T)
Reference rs80358082(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41226345T>A; NC_000017.10:g.41226345T>C
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000112378.1, RCV000164653.1,