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rs80357170

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;C) 1 BRCA1 variant of uncertain significance for breast cancer
(A;T) 6 BRCA1 variant considered pathogenic for breast cancer
Make rs80357170(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092854
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80357170
dbSNP (old)rs80357170
ClinGenrs80357170
ebirs80357170
HLIrs80357170
Exacrs80357170
Gnomadrs80357170
Varsomers80357170
Maprs80357170
PheGenIrs80357170
Biobankrs80357170
1000 genomesrs80357170
hgdprs80357170
ensemblrs80357170
gopubmedrs80357170
geneviewrs80357170
scholarrs80357170
googlers80357170
pharmgkbrs80357170
gwascentralrs80357170
openSNPrs80357170
23andMers80357170
23andMe allrs80357170
SNP Nexus

SNPshotrs80357170
SNPdbers80357170
MSV3drs80357170
GWAS Ctlgrs80357170
Max Magnitude6
ClinVar
Risk rs80357170(C;C) rs80357170(T;T)
Alt rs80357170(C;C) rs80357170(T;T)
Reference Rs80357170(A;A)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41244871T>A; NC_000017.10:g.41244871T>G
CLNSRC ClinVar
CLNACC RCV000031061.4, RCV000047923.2, RCV000111915.1,