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rs587777337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777337(C;C)
Make rs587777337(C;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position58742000
GeneMALT1
is asnp
is mentioned by
dbSNPrs587777337
ebirs587777337
HLIrs587777337
Exacrs587777337
Varsomers587777337
Maprs587777337
PheGenIrs587777337
hapmaprs587777337
1000 genomesrs587777337
hgdprs587777337
ensemblrs587777337
gopubmedrs587777337
geneviewrs587777337
scholarrs587777337
googlers587777337
pharmgkbrs587777337
gwascentralrs587777337
openSNPrs587777337
23andMers587777337
23andMe allrs587777337
SNP Nexus

SNPshotrs587777337
SNPdbers587777337
MSV3drs587777337
GWAS Ctlgrs587777337
Max Magnitude0
ClinVar
Risk rs587777337(C;C)
Alt rs587777337(C;C)
Reference rs587777337(G;G)
Significance Pathogenic
Disease Immunodeficiency 12
Variation info
Gene MALT1
CLNDBN Immunodeficiency 12
Reversed 0
HGVS NC_000018.9:g.56409232G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000114994.2,