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rs587776822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs587776822(-;-)
Make rs587776822(-;AG)
ReferenceGRCh38 38.1/142
Chromosome21
Position33421551
GeneIFNGR2
is asnp
is mentioned by
dbSNPrs587776822
ebirs587776822
HLIrs587776822
Exacrs587776822
Varsomers587776822
Maprs587776822
PheGenIrs587776822
hapmaprs587776822
1000 genomesrs587776822
hgdprs587776822
ensemblrs587776822
gopubmedrs587776822
geneviewrs587776822
scholarrs587776822
googlers587776822
pharmgkbrs587776822
gwascentralrs587776822
openSNPrs587776822
23andMers587776822
23andMe allrs587776822
SNP Nexus

SNPshotrs587776822
SNPdbers587776822
MSV3drs587776822
GWAS Ctlgrs587776822
Max Magnitude0
ClinVar
Risk rs587776822(;)
Alt rs587776822(;)
Reference rs587776822(AG;AG)
Significance Pathogenic
Disease Immunodeficiency 28
Variation info
Gene IFNGR2
CLNDBN Immunodeficiency 28
Reversed 0
HGVS NC_000021.8:g.34793858_34793859delAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000015847.27,