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rs72549322

From SNPedia

Orientationplus
Stabilizedplus
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
ReferenceGRCh38 38.1/141
Chromosome1
Position171103834
GeneFMO3
is asnp
is mentioned by
dbSNPrs72549322
ebirs72549322
HLIrs72549322
Exacrs72549322
Varsomers72549322
Maprs72549322
PheGenIrs72549322
hapmaprs72549322
1000 genomesrs72549322
hgdprs72549322
ensemblrs72549322
gopubmedrs72549322
geneviewrs72549322
scholarrs72549322
googlers72549322
pharmgkbrs72549322
gwascentralrs72549322
openSNPrs72549322
23andMers72549322
23andMe allrs72549322
SNP Nexus

SNPshotrs72549322
SNPdbers72549322
MSV3drs72549322
GWAS Ctlgrs72549322
Max Magnitude2
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]
OMIM136132
Desc
Variant0010
Relatedalso
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
CLNACC RCV000017706.25,