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rs80358165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 6 BRCA1 variant considered pathogenic for breast cancer
(C;G) 6 BRCA1 variant considered pathogenic for breast cancer
(G;G) 0 common in clinvar


Make rs80358165(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063869
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80358165
dbSNP (classic)rs80358165
ClinGenrs80358165
ebirs80358165
HLIrs80358165
Exacrs80358165
Gnomadrs80358165
Varsomers80358165
LitVarrs80358165
Maprs80358165
PheGenIrs80358165
Biobankrs80358165
1000 genomesrs80358165
hgdprs80358165
ensemblrs80358165
geneviewrs80358165
scholarrs80358165
googlers80358165
pharmgkbrs80358165
gwascentralrs80358165
openSNPrs80358165
23andMers80358165
SNPshotrs80358165
SNPdbers80358165
MSV3drs80358165
GWAS Ctlgrs80358165
Max Magnitude6
ClinVar
Risk rs80358165(A;A) rs80358165(C;C)
Alt rs80358165(A;A) rs80358165(C;C)
Reference Rs80358165(G;G)
Significance Other
Disease Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215886C>G; NC_000017.10:g.41215886C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000204262.3, RCV000048824.2, RCV000083217.4,