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rs80358096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs80358096(A;G)
Make rs80358096(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position43071240
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358096
ebirs80358096
HLIrs80358096
Exacrs80358096
Varsomers80358096
Maprs80358096
PheGenIrs80358096
hapmaprs80358096
1000 genomesrs80358096
hgdprs80358096
ensemblrs80358096
gopubmedrs80358096
geneviewrs80358096
scholarrs80358096
googlers80358096
pharmgkbrs80358096
gwascentralrs80358096
openSNPrs80358096
23andMers80358096
23andMe allrs80358096
SNP Nexus

SNPshotrs80358096
SNPdbers80358096
MSV3drs80358096
GWAS Ctlgrs80358096
Max Magnitude0
ClinVar
Risk rs80358096(G;G)
Alt rs80358096(G;G)
Reference rs80358096(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.41223257T>C
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000112382.1, RCV000131824.2,