rs4986997
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs4986997(A;T) |
Make rs4986997(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 18400414 |
Gene | NAT2 |
is a | snp |
is | mentioned by |
dbSNP | rs4986997 |
dbSNP (classic) | rs4986997 |
ClinGen | rs4986997 |
ebi | rs4986997 |
HLI | rs4986997 |
Exac | rs4986997 |
Gnomad | rs4986997 |
Varsome | rs4986997 |
LitVar | rs4986997 |
Map | rs4986997 |
PheGenI | rs4986997 |
Biobank | rs4986997 |
1000 genomes | rs4986997 |
hgdp | rs4986997 |
ensembl | rs4986997 |
geneview | rs4986997 |
scholar | rs4986997 |
rs4986997 | |
pharmgkb | rs4986997 |
gwascentral | rs4986997 |
openSNP | rs4986997 |
23andMe | rs4986997 |
SNPshot | rs4986997 |
SNPdbe | rs4986997 |
MSV3d | rs4986997 |
GWAS Ctlg | rs4986997 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 18680467] Structure/function evaluations of single nucleotide polymorphisms in human N-acetyltransferase 2.