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

rs367543038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs367543038(A;A)
Make rs367543038(A;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position90761001
GeneBLM
is asnp
is mentioned by
dbSNPrs367543038
ebirs367543038
HLIrs367543038
Exacrs367543038
Varsomers367543038
Maprs367543038
PheGenIrs367543038
hapmaprs367543038
1000 genomesrs367543038
hgdprs367543038
ensemblrs367543038
gopubmedrs367543038
geneviewrs367543038
scholarrs367543038
googlers367543038
pharmgkbrs367543038
gwascentralrs367543038
openSNPrs367543038
23andMers367543038
23andMe allrs367543038
SNP Nexus

SNPshotrs367543038
SNPdbers367543038
MSV3drs367543038
GWAS Ctlgrs367543038
Max Magnitude0
ClinVar
Risk rs367543038(A;A)
Alt rs367543038(A;A)
Reference rs367543038(T;T)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91304231T>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034891.1,