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rs387906765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906765(A;G)
Make rs387906765(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position190995143
GeneSTAT1
is asnp
is mentioned by
dbSNPrs387906765
ebirs387906765
HLIrs387906765
Exacrs387906765
Varsomers387906765
Maprs387906765
PheGenIrs387906765
hapmaprs387906765
1000 genomesrs387906765
hgdprs387906765
ensemblrs387906765
gopubmedrs387906765
geneviewrs387906765
scholarrs387906765
googlers387906765
pharmgkbrs387906765
gwascentralrs387906765
openSNPrs387906765
23andMers387906765
23andMe allrs387906765
SNP Nexus

SNPshotrs387906765
SNPdbers387906765
MSV3drs387906765
GWAS Ctlgrs387906765
Max Magnitude0
ClinVar
Risk rs387906765(G;G)
Alt rs387906765(G;G)
Reference rs387906765(A;A)
Significance Pathogenic
Disease Immunodeficiency 31C
Variation info
Gene STAT1
CLNDBN Immunodeficiency 31C
Reversed 1
HGVS NC_000002.11:g.191859869T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022993.5,