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rs80358018

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80358018(A;A)
Make rs80358018(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115780
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358018
ebirs80358018
HLIrs80358018
Exacrs80358018
Varsomers80358018
Maprs80358018
PheGenIrs80358018
hapmaprs80358018
1000 genomesrs80358018
hgdprs80358018
ensemblrs80358018
gopubmedrs80358018
geneviewrs80358018
scholarrs80358018
googlers80358018
pharmgkbrs80358018
gwascentralrs80358018
openSNPrs80358018
23andMers80358018
23andMe allrs80358018
SNP Nexus

SNPshotrs80358018
SNPdbers80358018
MSV3drs80358018
GWAS Ctlgrs80358018
Max Magnitude0
ClinVar
Risk rs80358018(A,C;A,C)
Alt rs80358018(A,C;A,C)
Reference rs80358018(G;G)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41267797C>G; NC_000017.10:g.41267797C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000049148.2, RCV000077185.3, RCV000131873.2, RCV000234498.1,