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rs730881428

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881428(G;G)
Make rs730881428(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position90760731
GeneBLM
is asnp
is mentioned by
dbSNPrs730881428
ebirs730881428
HLIrs730881428
Exacrs730881428
Varsomers730881428
Maprs730881428
PheGenIrs730881428
hapmaprs730881428
1000 genomesrs730881428
hgdprs730881428
ensemblrs730881428
gopubmedrs730881428
geneviewrs730881428
scholarrs730881428
googlers730881428
pharmgkbrs730881428
gwascentralrs730881428
openSNPrs730881428
23andMers730881428
23andMe allrs730881428
SNP Nexus

SNPshotrs730881428
SNPdbers730881428
MSV3drs730881428
GWAS Ctlgrs730881428
Max Magnitude0
ClinVar
Risk rs730881428(G;G)
Alt rs730881428(G;G)
Reference rs730881428(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.91303961T>G
CLNSRC
CLNACC RCV000159828.1,