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rs56379106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56379106(C;T)
Make rs56379106(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position18222237
GeneNAT1
is asnp
is mentioned by
dbSNPrs56379106
ebirs56379106
HLIrs56379106
Exacrs56379106
Varsomers56379106
Maprs56379106
PheGenIrs56379106
hapmaprs56379106
1000 genomesrs56379106
hgdprs56379106
ensemblrs56379106
gopubmedrs56379106
geneviewrs56379106
scholarrs56379106
googlers56379106
pharmgkbrs56379106
gwascentralrs56379106
openSNPrs56379106
23andMers56379106
23andMe allrs56379106
SNP Nexus

SNPshotrs56379106
SNPdbers56379106
MSV3drs56379106
GWAS Ctlgrs56379106
Max Magnitude0
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,