rs56379106
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs56379106(C;T) |
Make rs56379106(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 18222237 |
Gene | NAT1 |
is a | snp |
is | mentioned by |
dbSNP | rs56379106 |
dbSNP (classic) | rs56379106 |
ClinGen | rs56379106 |
ebi | rs56379106 |
HLI | rs56379106 |
Exac | rs56379106 |
Gnomad | rs56379106 |
Varsome | rs56379106 |
LitVar | rs56379106 |
Map | rs56379106 |
PheGenI | rs56379106 |
Biobank | rs56379106 |
1000 genomes | rs56379106 |
hgdp | rs56379106 |
ensembl | rs56379106 |
geneview | rs56379106 |
scholar | rs56379106 |
rs56379106 | |
pharmgkb | rs56379106 |
gwascentral | rs56379106 |
openSNP | rs56379106 |
23andMe | rs56379106 |
SNPshot | rs56379106 |
SNPdbe | rs56379106 |
MSV3d | rs56379106 |
GWAS Ctlg | rs56379106 |
Max Magnitude | 0 |
N-acetyltransferase NAT1*17 190C>T variant R64W, "slow metaboliser". [PMID 9511183, PMID 9682272]
ClinVar | |
---|---|
Risk | rs56379106(T;T) |
Alt | rs56379106(T;T) |
Reference | Rs56379106(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | NAT1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000008.10:g.18079746C>T |
CLNSRC | |
CLNACC | RCV000239134.1, |