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rs587776870

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776870(A;A)
Make rs587776870(A;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position190998247
GeneSTAT1
is asnp
is mentioned by
dbSNPrs587776870
ebirs587776870
HLIrs587776870
Exacrs587776870
Varsomers587776870
Maprs587776870
PheGenIrs587776870
hapmaprs587776870
1000 genomesrs587776870
hgdprs587776870
ensemblrs587776870
gopubmedrs587776870
geneviewrs587776870
scholarrs587776870
googlers587776870
pharmgkbrs587776870
gwascentralrs587776870
openSNPrs587776870
23andMers587776870
23andMe allrs587776870
SNP Nexus

SNPshotrs587776870
SNPdbers587776870
MSV3drs587776870
GWAS Ctlgrs587776870
Max Magnitude0
ClinVar
Risk rs587776870(A,C;A,C)
Alt rs587776870(A,C;A,C)
Reference rs587776870(G;G)
Significance Pathogenic
Disease Mycobacterial and viral infections
Variation info
Gene STAT1
CLNDBN Mycobacterial and viral infections, susceptibility to, autosomal recessive
Reversed 1
HGVS NC_000002.11:g.191862973C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022985.3,