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rs730881429

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881429(-;-)
Make rs730881429(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position90760758
GeneBLM
is asnp
is mentioned by
dbSNPrs730881429
ebirs730881429
HLIrs730881429
Exacrs730881429
Varsomers730881429
Maprs730881429
PheGenIrs730881429
hapmaprs730881429
1000 genomesrs730881429
hgdprs730881429
ensemblrs730881429
gopubmedrs730881429
geneviewrs730881429
scholarrs730881429
googlers730881429
pharmgkbrs730881429
gwascentralrs730881429
openSNPrs730881429
23andMers730881429
23andMe allrs730881429
SNP Nexus

SNPshotrs730881429
SNPdbers730881429
MSV3drs730881429
GWAS Ctlgrs730881429
Max Magnitude0
ClinVar
Risk rs730881429(;)
Alt rs730881429(;)
Reference rs730881429(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BLM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000015.9:g.91303988delC
CLNSRC
CLNACC RCV000159830.1,