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rs587779888

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779888(C;C)
Make rs587779888(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position90804359
GeneBLM
is asnp
is mentioned by
dbSNPrs587779888
ebirs587779888
HLIrs587779888
Exacrs587779888
Varsomers587779888
Maprs587779888
PheGenIrs587779888
hapmaprs587779888
1000 genomesrs587779888
hgdprs587779888
ensemblrs587779888
gopubmedrs587779888
geneviewrs587779888
scholarrs587779888
googlers587779888
pharmgkbrs587779888
gwascentralrs587779888
openSNPrs587779888
23andMers587779888
23andMe allrs587779888
SNP Nexus

SNPshotrs587779888
SNPdbers587779888
MSV3drs587779888
GWAS Ctlgrs587779888
Max Magnitude0
ClinVar
Risk rs587779888(C;C)
Alt rs587779888(C;C)
Reference rs587779888(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BLM
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.91347589G>C
CLNSRC
CLNACC RCV000115312.3,