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rs587779886

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779886(-;-)
Make rs587779886(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position90794359
GeneBLM
is asnp
is mentioned by
dbSNPrs587779886
ebirs587779886
HLIrs587779886
Exacrs587779886
Varsomers587779886
Maprs587779886
PheGenIrs587779886
hapmaprs587779886
1000 genomesrs587779886
hgdprs587779886
ensemblrs587779886
gopubmedrs587779886
geneviewrs587779886
scholarrs587779886
googlers587779886
pharmgkbrs587779886
gwascentralrs587779886
openSNPrs587779886
23andMers587779886
23andMe allrs587779886
SNP Nexus

SNPshotrs587779886
SNPdbers587779886
MSV3drs587779886
GWAS Ctlgrs587779886
Max Magnitude0
ClinVar
Risk rs587779886(;)
Alt rs587779886(;)
Reference rs587779886(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BLM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000015.9:g.91337589delT
CLNSRC
CLNACC RCV000115305.2,