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rs796065052

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796065052(A;A)
Make rs796065052(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position190986924
GeneSTAT1
is asnp
is mentioned by
dbSNPrs796065052
ebirs796065052
HLIrs796065052
Exacrs796065052
Varsomers796065052
Maprs796065052
PheGenIrs796065052
hapmaprs796065052
1000 genomesrs796065052
hgdprs796065052
ensemblrs796065052
gopubmedrs796065052
geneviewrs796065052
scholarrs796065052
googlers796065052
pharmgkbrs796065052
gwascentralrs796065052
openSNPrs796065052
23andMers796065052
23andMe allrs796065052
SNP Nexus

SNPshotrs796065052
SNPdbers796065052
MSV3drs796065052
GWAS Ctlgrs796065052
Max Magnitude0
ClinVar
Risk rs796065052(A;A)
Alt rs796065052(A;A)
Reference rs796065052(G;G)
Significance Pathogenic
Disease Immunodeficiency 31C
Variation info
Gene STAT1
CLNDBN Immunodeficiency 31C
Reversed 1
HGVS NC_000002.11:g.191851650C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190350.2,