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rs587783037

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783037(C;T)
Make rs587783037(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position90803577
GeneBLM
is asnp
is mentioned by
dbSNPrs587783037
ebirs587783037
HLIrs587783037
Exacrs587783037
Varsomers587783037
Maprs587783037
PheGenIrs587783037
hapmaprs587783037
1000 genomesrs587783037
hgdprs587783037
ensemblrs587783037
gopubmedrs587783037
geneviewrs587783037
scholarrs587783037
googlers587783037
pharmgkbrs587783037
gwascentralrs587783037
openSNPrs587783037
23andMers587783037
23andMe allrs587783037
SNP Nexus

SNPshotrs587783037
SNPdbers587783037
MSV3drs587783037
GWAS Ctlgrs587783037
Max Magnitude0
ClinVar
Risk rs587783037(T;T)
Alt rs587783037(T;T)
Reference rs587783037(C;C)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91346807C>T
CLNSRC
CLNACC RCV000144576.1,