Have questions? Visit https://www.reddit.com/r/SNPedia

rs367543036

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367543036(G;T)
Make rs367543036(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90763158
GeneBLM
is asnp
is mentioned by
dbSNPrs367543036
ebirs367543036
HLIrs367543036
Exacrs367543036
Varsomers367543036
Maprs367543036
PheGenIrs367543036
hapmaprs367543036
1000 genomesrs367543036
hgdprs367543036
ensemblrs367543036
gopubmedrs367543036
geneviewrs367543036
scholarrs367543036
googlers367543036
pharmgkbrs367543036
gwascentralrs367543036
openSNPrs367543036
23andMers367543036
23andMe allrs367543036
SNP Nexus

SNPshotrs367543036
SNPdbers367543036
MSV3drs367543036
GWAS Ctlgrs367543036
Max Magnitude0
ClinVar
Risk rs367543036(T;T)
Alt rs367543036(T;T)
Reference rs367543036(G;G)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91306388G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034892.1,