rs4076018
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4076018(A;A) |
Make rs4076018(A;T) |
Make rs4076018(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 115300189 |
Gene | NGF |
is a | snp |
is | mentioned by |
dbSNP | rs4076018 |
dbSNP (classic) | rs4076018 |
ClinGen | rs4076018 |
ebi | rs4076018 |
HLI | rs4076018 |
Exac | rs4076018 |
Gnomad | rs4076018 |
Varsome | rs4076018 |
LitVar | rs4076018 |
Map | rs4076018 |
PheGenI | rs4076018 |
Biobank | rs4076018 |
1000 genomes | rs4076018 |
hgdp | rs4076018 |
ensembl | rs4076018 |
geneview | rs4076018 |
scholar | rs4076018 |
rs4076018 | |
pharmgkb | rs4076018 |
gwascentral | rs4076018 |
openSNP | rs4076018 |
23andMe | rs4076018 |
SNPshot | rs4076018 |
SNPdbe | rs4076018 |
MSV3d | rs4076018 |
GWAS Ctlg | rs4076018 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 23792102] Phenotype variations affect genetic association studies of degenerative disc disease: conclusions of analysis of genetic association of 58 single nucleotide polymorphisms with highly specific phenotypes for disc degeneration in 332 subjects