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rs587776858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs587776858(-;-)
Make rs587776858(-;CTT)
ReferenceGRCh38 38.1/142
Chromosome6
Position137203577
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs587776858
ebirs587776858
HLIrs587776858
Exacrs587776858
Varsomers587776858
Maprs587776858
PheGenIrs587776858
hapmaprs587776858
1000 genomesrs587776858
hgdprs587776858
ensemblrs587776858
gopubmedrs587776858
geneviewrs587776858
scholarrs587776858
googlers587776858
pharmgkbrs587776858
gwascentralrs587776858
openSNPrs587776858
23andMers587776858
23andMe allrs587776858
SNP Nexus

SNPshotrs587776858
SNPdbers587776858
MSV3drs587776858
GWAS Ctlgrs587776858
Max Magnitude0
ClinVar
Risk rs587776858(;)
Alt rs587776858(;)
Reference rs587776858(CTT;CTT)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 0
HGVS NC_000006.11:g.137524714_137524716delCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000019547.31,