rs72549322
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(A;G) | 1 | likely to be an unaffected carrier of a trimethylaminuria allele |
(G;G) | 2 | trimethylaminuria & possible related issues; see discussion |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 171103834 |
Gene | FMO3 |
is a | snp |
is | mentioned by |
dbSNP | rs72549322 |
dbSNP (classic) | rs72549322 |
ClinGen | rs72549322 |
ebi | rs72549322 |
HLI | rs72549322 |
Exac | rs72549322 |
Gnomad | rs72549322 |
Varsome | rs72549322 |
LitVar | rs72549322 |
Map | rs72549322 |
PheGenI | rs72549322 |
Biobank | rs72549322 |
1000 genomes | rs72549322 |
hgdp | rs72549322 |
ensembl | rs72549322 |
geneview | rs72549322 |
scholar | rs72549322 |
rs72549322 | |
pharmgkb | rs72549322 |
gwascentral | rs72549322 |
openSNP | rs72549322 |
23andMe | rs72549322 |
SNPshot | rs72549322 |
SNPdbe | rs72549322 |
MSV3d | rs72549322 |
GWAS Ctlg | rs72549322 |
Max Magnitude | 2 |
rs72549322, also known as Asn61Ser, is a SNP in the FMO3 gene. In homozygous minor genotypes, it is likely to be lead to trimethylaminuria.[PMID 11191884]
ClinVar | |
---|---|
Risk | Rs72549322(G;G) |
Alt | Rs72549322(G;G) |
Reference | Rs72549322(A;A) |
Significance | Pathogenic |
Disease | Trimethylaminuria |
Variation | info |
Gene | FMO3 |
CLNDBN | Trimethylaminuria |
Reversed | 0 |
HGVS | NC_000001.10:g.171072975A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000017706.26, |