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rs80356914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356914(G;T)
Make rs80356914(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045759
GeneBRCA1
is asnp
is mentioned by
dbSNPrs80356914
ebirs80356914
HLIrs80356914
Exacrs80356914
Varsomers80356914
Maprs80356914
PheGenIrs80356914
hapmaprs80356914
1000 genomesrs80356914
hgdprs80356914
ensemblrs80356914
gopubmedrs80356914
geneviewrs80356914
scholarrs80356914
googlers80356914
pharmgkbrs80356914
gwascentralrs80356914
openSNPrs80356914
23andMers80356914
23andMe allrs80356914
SNP Nexus

SNPshotrs80356914
SNPdbers80356914
MSV3drs80356914
GWAS Ctlgrs80356914
Max Magnitude0
ClinVar
Risk rs80356914(A,T;A,T)
Alt rs80356914(A,T;A,T)
Reference rs80356914(G;G)
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.41197776C>A; NC_000017.10:g.41197776C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000031261.4, RCV000049030.2, RCV000049029.2, RCV000112692.1,