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rs375323253

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375323253(A;A)
Make rs375323253(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position613094
GeneIRF7
is asnp
is mentioned by
dbSNPrs375323253
ebirs375323253
HLIrs375323253
Exacrs375323253
Varsomers375323253
Maprs375323253
PheGenIrs375323253
hapmaprs375323253
1000 genomesrs375323253
hgdprs375323253
ensemblrs375323253
gopubmedrs375323253
geneviewrs375323253
scholarrs375323253
googlers375323253
pharmgkbrs375323253
gwascentralrs375323253
openSNPrs375323253
23andMers375323253
23andMe allrs375323253
SNP Nexus

SNPshotrs375323253
SNPdbers375323253
MSV3drs375323253
GWAS Ctlgrs375323253
Max Magnitude0
ClinVar
Risk rs375323253(A;A)
Alt rs375323253(A;A)
Reference rs375323253(G;G)
Significance Pathogenic
Disease Immunodeficiency 39
Variation info
Gene IRF7
CLNDBN Immunodeficiency 39
Reversed 0
HGVS NC_000011.9:g.613094G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170461.3,