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rs587776714

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776714(-;-)
Make rs587776714(-;T)
Make rs587776714(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position190976972
GeneSTAT1
is asnp
is mentioned by
dbSNPrs587776714
ebirs587776714
HLIrs587776714
Exacrs587776714
Varsomers587776714
Maprs587776714
PheGenIrs587776714
hapmaprs587776714
1000 genomesrs587776714
hgdprs587776714
ensemblrs587776714
gopubmedrs587776714
geneviewrs587776714
scholarrs587776714
googlers587776714
pharmgkbrs587776714
gwascentralrs587776714
openSNPrs587776714
23andMers587776714
23andMe allrs587776714
SNP Nexus

SNPshotrs587776714
SNPdbers587776714
MSV3drs587776714
GWAS Ctlgrs587776714
Max Magnitude0
ClinVar
Risk rs587776714(T;T)
Alt rs587776714(T;T)
Reference rs587776714(;)
Significance Pathogenic
Disease Mycobacterial and viral infections
Variation info
Gene STAT1
CLNDBN Mycobacterial and viral infections, susceptibility to, autosomal recessive
Reversed 0
HGVS NC_000002.11:g.191841698dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000009615.4,