Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777704(C;C)
Make rs587777704(C;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position190976881
GeneSTAT1
is asnp
is mentioned by
dbSNPrs587777704
ebirs587777704
HLIrs587777704
Exacrs587777704
Varsomers587777704
Maprs587777704
PheGenIrs587777704
hapmaprs587777704
1000 genomesrs587777704
hgdprs587777704
ensemblrs587777704
gopubmedrs587777704
geneviewrs587777704
scholarrs587777704
googlers587777704
pharmgkbrs587777704
gwascentralrs587777704
openSNPrs587777704
23andMers587777704
23andMe allrs587777704
SNP Nexus

SNPshotrs587777704
SNPdbers587777704
MSV3drs587777704
GWAS Ctlgrs587777704
Max Magnitude0
ClinVar
Risk rs587777704(C,T;C,T)
Alt rs587777704(C,T;C,T)
Reference rs587777704(A;A)
Significance Pathogenic
Disease Immunodeficiency 31a
Variation info
Gene STAT1
CLNDBN Immunodeficiency 31a
Reversed 1
HGVS NC_000002.11:g.191841607T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000144040.3,