rs4986996
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs4986996(A;A) |
Make rs4986996(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 18400367 |
Gene | NAT2 |
is a | snp |
is | mentioned by |
dbSNP | rs4986996 |
dbSNP (classic) | rs4986996 |
ClinGen | rs4986996 |
ebi | rs4986996 |
HLI | rs4986996 |
Exac | rs4986996 |
Gnomad | rs4986996 |
Varsome | rs4986996 |
LitVar | rs4986996 |
Map | rs4986996 |
PheGenI | rs4986996 |
Biobank | rs4986996 |
1000 genomes | rs4986996 |
hgdp | rs4986996 |
ensembl | rs4986996 |
geneview | rs4986996 |
scholar | rs4986996 |
rs4986996 | |
pharmgkb | rs4986996 |
gwascentral | rs4986996 |
openSNP | rs4986996 |
23andMe | rs4986996 |
SNPshot | rs4986996 |
SNPdbe | rs4986996 |
MSV3d | rs4986996 |
GWAS Ctlg | rs4986996 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 18680467] Structure/function evaluations of single nucleotide polymorphisms in human N-acetyltransferase 2.