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rs367543026

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs367543026(-;-)
Make rs367543026(-;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90749850
GeneBLM
is asnp
is mentioned by
dbSNPrs367543026
dbSNP (classic)rs367543026
ClinGenrs367543026
ebirs367543026
HLIrs367543026
Exacrs367543026
Gnomadrs367543026
Varsomers367543026
LitVarrs367543026
Maprs367543026
PheGenIrs367543026
Biobankrs367543026
1000 genomesrs367543026
hgdprs367543026
ensemblrs367543026
geneviewrs367543026
scholarrs367543026
googlers367543026
pharmgkbrs367543026
gwascentralrs367543026
openSNPrs367543026
23andMers367543026
SNPshotrs367543026
SNPdbers367543026
MSV3drs367543026
GWAS Ctlgrs367543026
Max Magnitude0
ClinVar
Risk rs367543026(-;-)
Alt rs367543026(-;-)
Reference Rs367543026(T;T)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91293080delT
CLNSRC ClinVar GeneReviews
CLNACC RCV000034917.1,