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

rs745372589

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745372589(A;G)
Make rs745372589(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position27443076
GeneIL21R
is asnp
is mentioned by
dbSNPrs745372589
ebirs745372589
HLIrs745372589
Exacrs745372589
Varsomers745372589
Maprs745372589
PheGenIrs745372589
hapmaprs745372589
1000 genomesrs745372589
hgdprs745372589
ensemblrs745372589
gopubmedrs745372589
geneviewrs745372589
scholarrs745372589
googlers745372589
pharmgkbrs745372589
gwascentralrs745372589
openSNPrs745372589
23andMers745372589
23andMe allrs745372589
SNP Nexus

SNPshotrs745372589
SNPdbers745372589
MSV3drs745372589
GWAS Ctlgrs745372589
Max Magnitude0
ClinVar
Risk rs745372589(G;G)
Alt rs745372589(G;G)
Reference rs745372589(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene IL21R
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000016.9:g.27454397A>G
CLNSRC
CLNACC RCV000210668.1,