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rs367543013

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs367543013(-;-)
Make rs367543013(-;CT)
ReferenceGRCh38 38.1/141
Chromosome15
Position90750040
GeneBLM
is asnp
is mentioned by
dbSNPrs367543013
ebirs367543013
HLIrs367543013
Exacrs367543013
Varsomers367543013
Maprs367543013
PheGenIrs367543013
hapmaprs367543013
1000 genomesrs367543013
hgdprs367543013
ensemblrs367543013
gopubmedrs367543013
geneviewrs367543013
scholarrs367543013
googlers367543013
pharmgkbrs367543013
gwascentralrs367543013
openSNPrs367543013
23andMers367543013
23andMe allrs367543013
SNP Nexus

SNPshotrs367543013
SNPdbers367543013
MSV3drs367543013
GWAS Ctlgrs367543013
Max Magnitude0
ClinVar
Risk rs367543013(;)
Alt rs367543013(;)
Reference rs367543013(CT;CT)
Significance Other
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91293270_91293271delCT
CLNSRC Counsyl
CLNACC RCV000034918.3,