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

rs367543039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367543039(A;A)
Make rs367543039(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position90782909
GeneBLM
is asnp
is mentioned by
dbSNPrs367543039
ebirs367543039
HLIrs367543039
Exacrs367543039
Varsomers367543039
Maprs367543039
PheGenIrs367543039
hapmaprs367543039
1000 genomesrs367543039
hgdprs367543039
ensemblrs367543039
gopubmedrs367543039
geneviewrs367543039
scholarrs367543039
googlers367543039
pharmgkbrs367543039
gwascentralrs367543039
openSNPrs367543039
23andMers367543039
23andMe allrs367543039
SNP Nexus

SNPshotrs367543039
SNPdbers367543039
MSV3drs367543039
GWAS Ctlgrs367543039
Max Magnitude0
ClinVar
Risk rs367543039(A;A)
Alt rs367543039(A;A)
Reference rs367543039(G;G)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91326139G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034898.1,