rs6334
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs6334(A;A) |
Make rs6334(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 156876441 |
Gene | NTRK1 |
is a | snp |
is | mentioned by |
dbSNP | rs6334 |
dbSNP (classic) | rs6334 |
ClinGen | rs6334 |
ebi | rs6334 |
HLI | rs6334 |
Exac | rs6334 |
Gnomad | rs6334 |
Varsome | rs6334 |
LitVar | rs6334 |
Map | rs6334 |
PheGenI | rs6334 |
Biobank | rs6334 |
1000 genomes | rs6334 |
hgdp | rs6334 |
ensembl | rs6334 |
geneview | rs6334 |
scholar | rs6334 |
rs6334 | |
pharmgkb | rs6334 |
gwascentral | rs6334 |
openSNP | rs6334 |
23andMe | rs6334 |
SNPshot | rs6334 |
SNPdbe | rs6334 |
MSV3d | rs6334 |
GWAS Ctlg | rs6334 |
GMAF | 0.2135 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23195334] Neurotrophin serum concentrations and polymorphisms of neurotrophins and their receptors in children with asthma
[PMID 21178826] Linkage and association study of neurotrophins and their receptors as novel susceptibility genes for childhood IgA nephropathy.
ClinVar | |
---|---|
Risk | rs6334(A;A) rs6334(C;C) |
Alt | rs6334(A;A) rs6334(C;C) |
Reference | Rs6334(G;G) |
Significance | Non-pathogenic |
Disease | Hereditary insensitivity to pain with anhidrosis |
Variation | info |
Gene | NTRK1 |
CLNDBN | Hereditary insensitivity to pain with anhidrosis |
Reversed | 0 |
HGVS | NC_000001.10:g.156846233G>A |
CLNSRC | |
CLNACC | RCV000366755.1, |