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rs80357104

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80357104(C;T)
Make rs80357104(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063361
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357104
ebirs80357104
HLIrs80357104
Exacrs80357104
Varsomers80357104
Maprs80357104
PheGenIrs80357104
hapmaprs80357104
1000 genomesrs80357104
hgdprs80357104
ensemblrs80357104
gopubmedrs80357104
geneviewrs80357104
scholarrs80357104
googlers80357104
pharmgkbrs80357104
gwascentralrs80357104
openSNPrs80357104
23andMers80357104
23andMe allrs80357104
SNP Nexus

SNPshotrs80357104
SNPdbers80357104
MSV3drs80357104
GWAS Ctlgrs80357104
Max Magnitude0
ClinVar
Risk rs80357104(T;T)
Alt rs80357104(T;T)
Reference rs80357104(C;C)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000017.10:g.41215378G>A
CLNSRC ClinVar
CLNACC RCV000048839.3, RCV000077606.4, RCV000214443.1, RCV000236284.1,