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

rs367543018

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367543018(-;-)
Make rs367543018(-;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position90804195
GeneBLM
is asnp
is mentioned by
dbSNPrs367543018
dbSNP (classic)rs367543018
ClinGenrs367543018
ebirs367543018
HLIrs367543018
Exacrs367543018
Gnomadrs367543018
Varsomers367543018
LitVarrs367543018
Maprs367543018
PheGenIrs367543018
Biobankrs367543018
1000 genomesrs367543018
hgdprs367543018
ensemblrs367543018
geneviewrs367543018
scholarrs367543018
googlers367543018
pharmgkbrs367543018
gwascentralrs367543018
openSNPrs367543018
23andMers367543018
SNPshotrs367543018
SNPdbers367543018
MSV3drs367543018
GWAS Ctlgrs367543018
Max Magnitude0
ClinVar
Risk rs367543018(-;-)
Alt rs367543018(-;-)
Reference Rs367543018(G;G)
Significance Pathogenic
Disease Bloom syndrome
Variation info
Gene BLM
CLNDBN Bloom syndrome
Reversed 0
HGVS NC_000015.9:g.91347425delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000034912.1,