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rs398122890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122890(-;-)
Make rs398122890(-;ACAATG)
Make rs398122890(ACAATG;ACAATG)
ReferenceGRCh38 38.1/141
Chromosome21
Position33421660
GeneIFNGR2
is asnp
is mentioned by
dbSNPrs398122890
ebirs398122890
HLIrs398122890
Exacrs398122890
Varsomers398122890
Maprs398122890
PheGenIrs398122890
hapmaprs398122890
1000 genomesrs398122890
hgdprs398122890
ensemblrs398122890
gopubmedrs398122890
geneviewrs398122890
scholarrs398122890
googlers398122890
pharmgkbrs398122890
gwascentralrs398122890
openSNPrs398122890
23andMers398122890
23andMe allrs398122890
SNP Nexus

SNPshotrs398122890
SNPdbers398122890
MSV3drs398122890
GWAS Ctlgrs398122890
Max Magnitude0
ClinVar
Risk rs398122890(TGACAA;TGACAA)
Alt rs398122890(TGACAA;TGACAA)
Reference rs398122890(;)
Significance Pathogenic
Disease Immunodeficiency 28
Variation info
Gene IFNGR2
CLNDBN Immunodeficiency 28
Reversed 0
HGVS NC_000021.8:g.34793962_34793967dupACAATG
CLNSRC OMIM Allelic Variant
CLNACC RCV000030825.27,