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rs80356977

From SNPedia

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


Make rs80356977(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045735
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356977
dbSNP (old)rs80356977
ClinGenrs80356977
ebirs80356977
HLIrs80356977
Exacrs80356977
Gnomadrs80356977
Varsomers80356977
Maprs80356977
PheGenIrs80356977
Biobankrs80356977
1000 genomesrs80356977
hgdprs80356977
ensemblrs80356977
gopubmedrs80356977
geneviewrs80356977
scholarrs80356977
googlers80356977
pharmgkbrs80356977
gwascentralrs80356977
openSNPrs80356977
23andMers80356977
23andMe allrs80356977
SNP Nexus

SNPshotrs80356977
SNPdbers80356977
MSV3drs80356977
GWAS Ctlgrs80356977
Max Magnitude6
ClinVar
Risk rs80356977(A;A) rs80356977(G;G)
Alt rs80356977(A;A) rs80356977(G;G)
Reference Rs80356977(C;C)
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.41197752G>C; NC_000017.10:g.41197752G>T
CLNSRC ClinVar
CLNACC RCV000256729.2, RCV000049041.2, RCV000112698.3,