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rs80356967

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356967(A;A)
Make rs80356967(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104953
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356967
ebirs80356967
HLIrs80356967
Exacrs80356967
Varsomers80356967
Maprs80356967
PheGenIrs80356967
hapmaprs80356967
1000 genomesrs80356967
hgdprs80356967
ensemblrs80356967
gopubmedrs80356967
geneviewrs80356967
scholarrs80356967
googlers80356967
pharmgkbrs80356967
gwascentralrs80356967
openSNPrs80356967
23andMers80356967
23andMe allrs80356967
SNP Nexus

SNPshotrs80356967
SNPdbers80356967
MSV3drs80356967
GWAS Ctlgrs80356967
Max Magnitude0
ClinVar
Risk rs80356967(A,G;A,G)
Alt rs80356967(A,G;A,G)
Reference rs80356967(C;C)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41256970G>C; NC_000017.10:g.41256970G>T
CLNSRC ClinVar
CLNACC RCV000159936.1, RCV000047740.2, RCV000077507.3,