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rs786205223

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205223(G;G)
Make rs786205223(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position613215
GeneIRF7
is asnp
is mentioned by
dbSNPrs786205223
ebirs786205223
HLIrs786205223
Exacrs786205223
Varsomers786205223
Maprs786205223
PheGenIrs786205223
hapmaprs786205223
1000 genomesrs786205223
hgdprs786205223
ensemblrs786205223
gopubmedrs786205223
geneviewrs786205223
scholarrs786205223
googlers786205223
pharmgkbrs786205223
gwascentralrs786205223
openSNPrs786205223
23andMers786205223
23andMe allrs786205223
SNP Nexus

SNPshotrs786205223
SNPdbers786205223
MSV3drs786205223
GWAS Ctlgrs786205223
Max Magnitude0
ClinVar
Risk rs786205223(G;G)
Alt rs786205223(G;G)
Reference rs786205223(T;T)
Significance Pathogenic
Disease Immunodeficiency 39
Variation info
Gene IRF7
CLNDBN Immunodeficiency 39
Reversed 1
HGVS NC_000011.9:g.613215A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000170460.3,