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rs387906572

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906572(A;A)
Make rs387906572(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position137204432
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs387906572
ebirs387906572
HLIrs387906572
Exacrs387906572
Varsomers387906572
Maprs387906572
PheGenIrs387906572
hapmaprs387906572
1000 genomesrs387906572
hgdprs387906572
ensemblrs387906572
gopubmedrs387906572
geneviewrs387906572
scholarrs387906572
googlers387906572
pharmgkbrs387906572
gwascentralrs387906572
openSNPrs387906572
23andMers387906572
23andMe allrs387906572
SNP Nexus

SNPshotrs387906572
SNPdbers387906572
MSV3drs387906572
GWAS Ctlgrs387906572
Max Magnitude0
ClinVar
Risk rs387906572(A;A)
Alt rs387906572(A;A)
Reference rs387906572(C;C)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 1
HGVS NC_000006.11:g.137525569G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019537.30,