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rs121912715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121912715(A;A)
Make rs121912715(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position137206981
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs121912715
ebirs121912715
HLIrs121912715
Exacrs121912715
Varsomers121912715
Maprs121912715
PheGenIrs121912715
hapmaprs121912715
1000 genomesrs121912715
hgdprs121912715
ensemblrs121912715
gopubmedrs121912715
geneviewrs121912715
scholarrs121912715
googlers121912715
pharmgkbrs121912715
gwascentralrs121912715
openSNPrs121912715
23andMers121912715
23andMe allrs121912715
SNP Nexus

SNPshotrs121912715
SNPdbers121912715
MSV3drs121912715
GWAS Ctlgrs121912715
Max Magnitude0
OMIM107470
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121912715(G;G)
Alt rs121912715(G;G)
Reference rs121912715(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.137528118A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019546.27,