rs3135941
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs3135941(C;C) |
Make rs3135941(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 48466268 |
Gene | TREX1 |
is a | snp |
is | mentioned by |
dbSNP | rs3135941 |
dbSNP (classic) | rs3135941 |
ClinGen | rs3135941 |
ebi | rs3135941 |
HLI | rs3135941 |
Exac | rs3135941 |
Gnomad | rs3135941 |
Varsome | rs3135941 |
LitVar | rs3135941 |
Map | rs3135941 |
PheGenI | rs3135941 |
Biobank | rs3135941 |
1000 genomes | rs3135941 |
hgdp | rs3135941 |
ensembl | rs3135941 |
geneview | rs3135941 |
scholar | rs3135941 |
rs3135941 | |
pharmgkb | rs3135941 |
gwascentral | rs3135941 |
openSNP | rs3135941 |
23andMe | rs3135941 |
SNPshot | rs3135941 |
SNPdbe | rs3135941 |
MSV3d | rs3135941 |
GWAS Ctlg | rs3135941 |
Max Magnitude | 0 |
? | (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, |