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rs397514685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514685(G;T)
Make rs397514685(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position27444636
GeneIL21R
is asnp
is mentioned by
dbSNPrs397514685
ebirs397514685
HLIrs397514685
Exacrs397514685
Varsomers397514685
Maprs397514685
PheGenIrs397514685
hapmaprs397514685
1000 genomesrs397514685
hgdprs397514685
ensemblrs397514685
gopubmedrs397514685
geneviewrs397514685
scholarrs397514685
googlers397514685
pharmgkbrs397514685
gwascentralrs397514685
openSNPrs397514685
23andMers397514685
23andMe allrs397514685
SNP Nexus

SNPshotrs397514685
SNPdbers397514685
MSV3drs397514685
GWAS Ctlgrs397514685
Max Magnitude0
ClinVar
Risk rs397514685(T;T)
Alt rs397514685(T;T)
Reference rs397514685(G;G)
Significance Pathogenic
Disease IL21R immunodeficiency
Variation info
Gene IL21R
CLNDBN IL21R immunodeficiency
Reversed 0
HGVS NC_000016.9:g.27455957G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000035024.3,