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rs367543029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367543029(C;C)
Make rs367543029(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position90794311
GeneBLM
is asnp
is mentioned by
dbSNPrs367543029
ebirs367543029
HLIrs367543029
Exacrs367543029
Varsomers367543029
Maprs367543029
PheGenIrs367543029
hapmaprs367543029
1000 genomesrs367543029
hgdprs367543029
ensemblrs367543029
gopubmedrs367543029
geneviewrs367543029
scholarrs367543029
googlers367543029
pharmgkbrs367543029
gwascentralrs367543029
openSNPrs367543029
23andMers367543029
23andMe allrs367543029
SNP Nexus

SNPshotrs367543029
SNPdbers367543029
MSV3drs367543029
GWAS Ctlgrs367543029
Max Magnitude0
ClinVar
Risk rs367543029(C;C)
Alt rs367543029(C;C)
Reference rs367543029(G;G)
Significance Pathogenic
Disease Bloom syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000015.9:g.91337541G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034904.1, RCV000159829.1,