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rs367543031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs367543031(C;T)
Make rs367543031(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90809232
GeneBLM
is asnp
is mentioned by
dbSNPrs367543031
ebirs367543031
HLIrs367543031
Exacrs367543031
Varsomers367543031
Maprs367543031
PheGenIrs367543031
hapmaprs367543031
1000 genomesrs367543031
hgdprs367543031
ensemblrs367543031
gopubmedrs367543031
geneviewrs367543031
scholarrs367543031
googlers367543031
pharmgkbrs367543031
gwascentralrs367543031
openSNPrs367543031
23andMers367543031
23andMe allrs367543031
SNP Nexus

SNPshotrs367543031
SNPdbers367543031
MSV3drs367543031
GWAS Ctlgrs367543031
Max Magnitude0
ClinVar
Risk rs367543031(T;T)
Alt rs367543031(T;T)
Reference rs367543031(C;C)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91352462C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034915.1,