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rs587777338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777338(A;G)
Make rs587777338(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position122620866
GeneIL21, IL21-AS1
is asnp
is mentioned by
dbSNPrs587777338
ebirs587777338
HLIrs587777338
Exacrs587777338
Varsomers587777338
Maprs587777338
PheGenIrs587777338
hapmaprs587777338
1000 genomesrs587777338
hgdprs587777338
ensemblrs587777338
gopubmedrs587777338
geneviewrs587777338
scholarrs587777338
googlers587777338
pharmgkbrs587777338
gwascentralrs587777338
openSNPrs587777338
23andMers587777338
23andMe allrs587777338
SNP Nexus

SNPshotrs587777338
SNPdbers587777338
MSV3drs587777338
GWAS Ctlgrs587777338
Max Magnitude0
ClinVar
Risk rs587777338(G;G)
Alt rs587777338(G;G)
Reference rs587777338(A;A)
Significance Pathogenic
Disease Common variable immunodeficiency 11
Variation info
Gene IL21 IL21-AS1
CLNDBN Common variable immunodeficiency 11
Reversed 0
HGVS NC_000004.11:g.123542021A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000114995.6,