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rs863224765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224765(C;C)
Make rs863224765(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position43051086
GeneBRCA1
is asnp
is mentioned by
dbSNPrs863224765
dbSNP (classic)rs863224765
ClinGenrs863224765
ebirs863224765
HLIrs863224765
Exacrs863224765
Gnomadrs863224765
Varsomers863224765
LitVarrs863224765
Maprs863224765
PheGenIrs863224765
Biobankrs863224765
1000 genomesrs863224765
hgdprs863224765
ensemblrs863224765
geneviewrs863224765
scholarrs863224765
googlers863224765
pharmgkbrs863224765
gwascentralrs863224765
openSNPrs863224765
23andMers863224765
SNPshotrs863224765
SNPdbers863224765
MSV3drs863224765
GWAS Ctlgrs863224765
Max Magnitude0
ClinVar
Risk rs863224765(C;C) rs863224765(T;T)
Alt rs863224765(C;C) rs863224765(T;T)
Reference Rs863224765(G;G)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41203103C>A; NC_000017.10:g.41203103C>G
CLNSRC
CLNACC RCV000477771.1, RCV000199320.1,