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rs587777335

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777335(C;C)
Make rs587777335(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position32279728
GeneLCK
is asnp
is mentioned by
dbSNPrs587777335
ebirs587777335
HLIrs587777335
Exacrs587777335
Varsomers587777335
Maprs587777335
PheGenIrs587777335
hapmaprs587777335
1000 genomesrs587777335
hgdprs587777335
ensemblrs587777335
gopubmedrs587777335
geneviewrs587777335
scholarrs587777335
googlers587777335
pharmgkbrs587777335
gwascentralrs587777335
openSNPrs587777335
23andMers587777335
23andMe allrs587777335
SNP Nexus

SNPshotrs587777335
SNPdbers587777335
MSV3drs587777335
GWAS Ctlgrs587777335
Max Magnitude0
ClinVar
Risk rs587777335(C;C)
Alt rs587777335(C;C)
Reference rs587777335(T;T)
Significance Pathogenic
Disease Immunodeficiency 22
Variation info
Gene LCK
CLNDBN Immunodeficiency 22
Reversed 0
HGVS NC_000001.10:g.32745329T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000114989.2,