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rs80357101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80357101(C;C)
Make rs80357101(C;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092107
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357101
ebirs80357101
HLIrs80357101
Exacrs80357101
Varsomers80357101
Maprs80357101
PheGenIrs80357101
hapmaprs80357101
1000 genomesrs80357101
hgdprs80357101
ensemblrs80357101
gopubmedrs80357101
geneviewrs80357101
scholarrs80357101
googlers80357101
pharmgkbrs80357101
gwascentralrs80357101
openSNPrs80357101
23andMers80357101
23andMe allrs80357101
SNP Nexus

SNPshotrs80357101
SNPdbers80357101
MSV3drs80357101
GWAS Ctlgrs80357101
Max Magnitude0
ClinVar
Risk rs80357101(C;C)
Alt rs80357101(C;C)
Reference rs80357101(G;G)
Significance Other
Disease Familial cancer of breast Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41244124C>G
CLNSRC ClinVar
CLNACC RCV000048190.2, RCV000077548.4, RCV000221866.1,