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rs387906593

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906593(A;A)
Make rs387906593(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position137219326
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs387906593
ebirs387906593
HLIrs387906593
Exacrs387906593
Varsomers387906593
Maprs387906593
PheGenIrs387906593
hapmaprs387906593
1000 genomesrs387906593
hgdprs387906593
ensemblrs387906593
gopubmedrs387906593
geneviewrs387906593
scholarrs387906593
googlers387906593
pharmgkbrs387906593
gwascentralrs387906593
openSNPrs387906593
23andMers387906593
23andMe allrs387906593
SNP Nexus

SNPshotrs387906593
SNPdbers387906593
MSV3drs387906593
GWAS Ctlgrs387906593
Max Magnitude0
ClinVar
Risk rs387906593(A,G;A,G)
Alt rs387906593(A,G;A,G)
Reference rs387906593(T;T)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 1
HGVS NC_000006.11:g.137540463A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022447.30,