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rs80356857

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356857(A;A)
Make rs80356857(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43090944
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356857
ebirs80356857
HLIrs80356857
Exacrs80356857
Varsomers80356857
Maprs80356857
PheGenIrs80356857
hapmaprs80356857
1000 genomesrs80356857
hgdprs80356857
ensemblrs80356857
gopubmedrs80356857
geneviewrs80356857
scholarrs80356857
googlers80356857
pharmgkbrs80356857
gwascentralrs80356857
openSNPrs80356857
23andMers80356857
23andMe allrs80356857
SNP Nexus

SNPshotrs80356857
SNPdbers80356857
MSV3drs80356857
GWAS Ctlgrs80356857
Max Magnitude0
ClinVar
Risk rs80356857(A;A)
Alt rs80356857(A;A)
Reference rs80356857(G;G)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41242961C>G; NC_000017.10:g.41242961C>T
CLNSRC ClinVar
CLNACC RCV000215792.1, RCV000048477.2, RCV000112286.1,