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rs587776854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587776854(-;GTAA)
Make rs587776854(GTAA;GTAA)
ReferenceGRCh38 38.1/142
Chromosome6
Position137207059
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs587776854
dbSNP (classic)rs587776854
ClinGenrs587776854
ebirs587776854
HLIrs587776854
Exacrs587776854
Gnomadrs587776854
Varsomers587776854
LitVarrs587776854
Maprs587776854
PheGenIrs587776854
Biobankrs587776854
1000 genomesrs587776854
hgdprs587776854
ensemblrs587776854
geneviewrs587776854
scholarrs587776854
googlers587776854
pharmgkbrs587776854
gwascentralrs587776854
openSNPrs587776854
23andMers587776854
SNPshotrs587776854
SNPdbers587776854
MSV3drs587776854
GWAS Ctlgrs587776854
Max Magnitude0
ClinVar
Risk rs587776854(GTAA;GTAA)
Alt rs587776854(GTAA;GTAA)
Reference Rs587776854(-;-)
Significance Pathogenic
Disease Disseminated atypical mycobacterial infection
Variation info
Gene IFNGR1
CLNDBN Disseminated atypical mycobacterial infection
Reversed 0
HGVS NC_000006.11:g.137528193_137528196dupGTAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000019541.31,