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rs367543032

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs367543032(A;T)
Make rs367543032(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90794338
GeneBLM
is asnp
is mentioned by
dbSNPrs367543032
ebirs367543032
HLIrs367543032
Exacrs367543032
Varsomers367543032
Maprs367543032
PheGenIrs367543032
hapmaprs367543032
1000 genomesrs367543032
hgdprs367543032
ensemblrs367543032
gopubmedrs367543032
geneviewrs367543032
scholarrs367543032
googlers367543032
pharmgkbrs367543032
gwascentralrs367543032
openSNPrs367543032
23andMers367543032
23andMe allrs367543032
SNP Nexus

SNPshotrs367543032
SNPdbers367543032
MSV3drs367543032
GWAS Ctlgrs367543032
Max Magnitude0
ClinVar
Risk rs367543032(G,T;G,T)
Alt rs367543032(G,T;G,T)
Reference rs367543032(A;A)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91337568A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034905.1,