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rs3799488

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3799488(C;C)
Make rs3799488(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position137198643
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs3799488
dbSNP (classic)rs3799488
ClinGenrs3799488
ebirs3799488
HLIrs3799488
Exacrs3799488
Gnomadrs3799488
Varsomers3799488
LitVarrs3799488
Maprs3799488
PheGenIrs3799488
Biobankrs3799488
1000 genomesrs3799488
hgdprs3799488
ensemblrs3799488
geneviewrs3799488
scholarrs3799488
googlers3799488
pharmgkbrs3799488
gwascentralrs3799488
openSNPrs3799488
23andMers3799488
SNPshotrs3799488
SNPdbers3799488
MSV3drs3799488
GWAS Ctlgrs3799488
GMAF0.1382
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 21859832OA-icon.png] Interferon-signaling pathway: associations with colon and rectal cancer risk and subsequent survival


[PMID 16449530OA-icon.png] Cytokine polymorphisms in the Th1/Th2 pathway and susceptibility to non-Hodgkin lymphoma.


[PMID 17327408OA-icon.png] Prognostic significance of host immune gene polymorphisms in follicular lymphoma survival.


[PMID 18633131OA-icon.png] Host immune gene polymorphisms in combination with clinical and demographic factors predict late survival in diffuse large B-cell lymphoma patients in the pre-rituximab era.


[PMID 19066394OA-icon.png] Organochlorine exposure, immune gene variation, and risk of non-Hodgkin lymphoma.


[PMID 19356949OA-icon.png] Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies.


ClinVar
Risk rs3799488(C;C)
Alt rs3799488(C;C)
Reference Rs3799488(T;T)
Significance Non-pathogenic
Disease Familial Atypical Mycobacteriosis not specified
Variation info
Gene IFNGR1
CLNDBN Familial Atypical Mycobacteriosis, Autosomal Recessive not specified
Reversed 0
HGVS NC_000006.11:g.137519780T>C
CLNSRC
CLNACC RCV000370631.1, RCV000454477.1,