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rs869320776

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320776(-;-)
Make rs869320776(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093931
GeneBRCA1
is asnp
is mentioned by
dbSNPrs869320776
ebirs869320776
HLIrs869320776
Exacrs869320776
Varsomers869320776
Maprs869320776
PheGenIrs869320776
hapmaprs869320776
1000 genomesrs869320776
hgdprs869320776
ensemblrs869320776
gopubmedrs869320776
geneviewrs869320776
scholarrs869320776
googlers869320776
pharmgkbrs869320776
gwascentralrs869320776
openSNPrs869320776
23andMers869320776
23andMe allrs869320776
SNP Nexus

SNPshotrs869320776
SNPdbers869320776
MSV3drs869320776
GWAS Ctlgrs869320776
Max Magnitude0
ClinVar
Risk rs869320776(;)
Alt rs869320776(;)
Reference rs869320776(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245948delG
CLNSRC
CLNACC RCV000210963.1,