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rs587776856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATTA;ATTA) 0 common in clinvar
(TAATC;TAATC) 0 common in clinvar
Make rs587776856(-;-)
Make rs587776856(-;ATTA)
ReferenceGRCh38 38.1/142
Chromosome6
Position137200920
GeneIFNGR1
is asnp
is mentioned by
dbSNPrs587776856
ebirs587776856
HLIrs587776856
Exacrs587776856
Varsomers587776856
Maprs587776856
PheGenIrs587776856
hapmaprs587776856
1000 genomesrs587776856
hgdprs587776856
ensemblrs587776856
gopubmedrs587776856
geneviewrs587776856
scholarrs587776856
googlers587776856
pharmgkbrs587776856
gwascentralrs587776856
openSNPrs587776856
23andMers587776856
23andMe allrs587776856
SNP Nexus

SNPshotrs587776856
SNPdbers587776856
MSV3drs587776856
GWAS Ctlgrs587776856
Max Magnitude0
ClinVar
Risk rs587776856(ATTAC,C;ATTAC,C)
Alt rs587776856(ATTAC,C;ATTAC,C)
Reference rs587776856(TAATC;TAATC)
Significance Pathogenic
Disease Immunodeficiency 27b
Variation info
Gene IFNGR1
CLNDBN Immunodeficiency 27b
Reversed 1
HGVS NC_000006.11:g.137522057_137522060delATTA
CLNSRC OMIM Allelic Variant
CLNACC RCV000019543.32,