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rs749956849

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs749956849(-;-)
Make rs749956849(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position137204355
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs749956849
ebirs749956849
HLIrs749956849
Exacrs749956849
Varsomers749956849
Maprs749956849
PheGenIrs749956849
hapmaprs749956849
1000 genomesrs749956849
hgdprs749956849
ensemblrs749956849
gopubmedrs749956849
geneviewrs749956849
scholarrs749956849
googlers749956849
pharmgkbrs749956849
gwascentralrs749956849
openSNPrs749956849
23andMers749956849
23andMe allrs749956849
SNP Nexus

SNPshotrs749956849
SNPdbers749956849
MSV3drs749956849
GWAS Ctlgrs749956849
Max Magnitude0
ClinVar
Risk rs749956849(;)
Alt rs749956849(;)
Reference rs749956849(A;A)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 0
HGVS NC_000006.11:g.137525492delA
CLNSRC
CLNACC RCV000190596.1,