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rs587776855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776855(C;T)
Make rs587776855(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position137206962
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs587776855
ebirs587776855
HLIrs587776855
Exacrs587776855
Varsomers587776855
Maprs587776855
PheGenIrs587776855
hapmaprs587776855
1000 genomesrs587776855
hgdprs587776855
ensemblrs587776855
gopubmedrs587776855
geneviewrs587776855
scholarrs587776855
googlers587776855
pharmgkbrs587776855
gwascentralrs587776855
openSNPrs587776855
23andMers587776855
23andMe allrs587776855
SNP Nexus

SNPshotrs587776855
SNPdbers587776855
MSV3drs587776855
GWAS Ctlgrs587776855
Max Magnitude0
ClinVar
Risk rs587776855(C,T;C,T)
Alt rs587776855(C,T;C,T)
Reference rs587776855(G;G)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 1
HGVS NC_000006.11:g.137528099C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019542.32,