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rs587781258

From SNPedia

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


Make rs587781258(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43057124
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587781258
ClinGenrs587781258
ebirs587781258
HLIrs587781258
Exacrs587781258
Varsomers587781258
Maprs587781258
PheGenIrs587781258
hapmaprs587781258
1000 genomesrs587781258
hgdprs587781258
ensemblrs587781258
gopubmedrs587781258
geneviewrs587781258
scholarrs587781258
googlers587781258
pharmgkbrs587781258
gwascentralrs587781258
openSNPrs587781258
23andMers587781258
23andMe allrs587781258
SNP Nexus

SNPshotrs587781258
SNPdbers587781258
MSV3drs587781258
GWAS Ctlgrs587781258
Max Magnitude6
ClinVar
Risk
Alt
Reference Rs587781258(A;A)
Significance Pathogenic
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.41209141delT
CLNSRC VariO
CLNACC RCV000128632.1, RCV000241143.1,