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rs587781258

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781258(-;-)
Make rs587781258(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43057124
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587781258
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 Magnitude0
ClinVar
Risk rs587781258(;)
Alt rs587781258(;)
Reference rs587781258(A;A)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41209141delT
CLNSRC VariO
CLNACC RCV000128632.1,