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rs587776860

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs587776860(-;-)
Make rs587776860(-;A)
ReferenceGRCh38 38.1/142
Chromosome6
Position137200948
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs587776860
ebirs587776860
HLIrs587776860
Exacrs587776860
Varsomers587776860
Maprs587776860
PheGenIrs587776860
hapmaprs587776860
1000 genomesrs587776860
hgdprs587776860
ensemblrs587776860
gopubmedrs587776860
geneviewrs587776860
scholarrs587776860
googlers587776860
pharmgkbrs587776860
gwascentralrs587776860
openSNPrs587776860
23andMers587776860
23andMe allrs587776860
SNP Nexus

SNPshotrs587776860
SNPdbers587776860
MSV3drs587776860
GWAS Ctlgrs587776860
Max Magnitude0
ClinVar
Risk rs587776860(AC,C;AC,C)
Alt rs587776860(AC,C;AC,C)
Reference rs587776860(TC;TC)
Significance Pathogenic
Disease Immunodeficiency 27b
Variation info
Gene IFNGR1
CLNDBN Immunodeficiency 27b
Reversed 1
HGVS NC_000006.11:g.137522085delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000019552.30,