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rs587781825

From SNPedia

Orientationminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs587781825(-;-)
Make rs587781825(-;GC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43051084
GeneBRCA1
is asnp
is mentioned by
dbSNPrs587781825
ebirs587781825
HLIrs587781825
Exacrs587781825
Varsomers587781825
Maprs587781825
PheGenIrs587781825
hapmaprs587781825
1000 genomesrs587781825
hgdprs587781825
ensemblrs587781825
gopubmedrs587781825
geneviewrs587781825
scholarrs587781825
googlers587781825
pharmgkbrs587781825
gwascentralrs587781825
openSNPrs587781825
23andMers587781825
23andMe allrs587781825
SNP Nexus

SNPshotrs587781825
SNPdbers587781825
MSV3drs587781825
GWAS Ctlgrs587781825
Max Magnitude0
ClinVar
Risk rs587781825(;)
Alt rs587781825(;)
Reference rs587781825(GC;GC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41203101_41203102delGC
CLNSRC
CLNACC RCV000130106.2,