rs745372589

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs745372589(A;G)

Make rs745372589(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

27443076

Gene

IL21R

is a	snp
is	mentioned by
dbSNP	rs745372589
dbSNP (classic)	rs745372589
ClinGen	rs745372589
ebi	rs745372589
HLI	rs745372589
Exac	rs745372589
Gnomad	rs745372589
Varsome	rs745372589
LitVar	rs745372589
Map	rs745372589
PheGenI	rs745372589
Biobank	rs745372589
1000 genomes	rs745372589
hgdp	rs745372589
ensembl	rs745372589
geneview	rs745372589
scholar	rs745372589
google	rs745372589
pharmgkb	rs745372589
gwascentral	rs745372589
openSNP	rs745372589
23andMe	rs745372589
SNPshot	rs745372589
SNPdbe	rs745372589
MSV3d	rs745372589
GWAS Ctlg	rs745372589

Max Magnitude

0

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,