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rs3135941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3135941(C;C)
Make rs3135941(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position48466268
GeneTREX1
is asnp
is mentioned by
dbSNPrs3135941
dbSNP (classic)rs3135941
ClinGenrs3135941
ebirs3135941
HLIrs3135941
Exacrs3135941
Gnomadrs3135941
Varsomers3135941
LitVarrs3135941
Maprs3135941
PheGenIrs3135941
Biobankrs3135941
1000 genomesrs3135941
hgdprs3135941
ensemblrs3135941
geneviewrs3135941
scholarrs3135941
googlers3135941
pharmgkbrs3135941
gwascentralrs3135941
openSNPrs3135941
23andMers3135941
SNPshotrs3135941
SNPdbers3135941
MSV3drs3135941
GWAS Ctlgrs3135941
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25162766] Genetic variation in Trex1 affects HIV-1 disease progression


ClinVar
Risk rs3135941(A;A) rs3135941(C;C)
Alt rs3135941(A;A) rs3135941(C;C)
Reference Rs3135941(T;T)
Significance Non-pathogenic
Disease Aicardi Goutieres syndrome Vasculopathy
Variation info
Gene ATRIP TREX1
CLNDBN Aicardi Goutieres syndrome Vasculopathy, retinal, with cerebral leukodystrophy
Reversed 0
HGVS NC_000003.11:g.48507667T>C
CLNSRC
CLNACC RCV000352883.1, RCV000406520.1,