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rs909530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs909530(C;T)
Make rs909530(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position171114034
GeneFMO3
is asnp
is mentioned by
dbSNPrs909530
dbSNP (classic)rs909530
ClinGenrs909530
ebirs909530
HLIrs909530
Exacrs909530
Gnomadrs909530
Varsomers909530
LitVarrs909530
Maprs909530
PheGenIrs909530
Biobankrs909530
1000 genomesrs909530
hgdprs909530
ensemblrs909530
geneviewrs909530
scholarrs909530
googlers909530
pharmgkbrs909530
gwascentralrs909530
openSNPrs909530
23andMers909530
SNPshotrs909530
SNPdbers909530
MSV3drs909530
GWAS Ctlgrs909530
GMAF0.3338
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24173915] Effects of single nucleotide polymorphisms of FMO3 and FMO6 genes on pharmacokinetic characteristics of sulindac sulfide in premature labor


[PMID 15858076] Discovery of novel flavin-containing monooxygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants.


ClinVar
Risk rs909530(T;T)
Alt rs909530(T;T)
Reference Rs909530(C;C)
Significance Non-pathogenic
Disease not specified Trimethylaminuria
Variation info
Gene FMO3
CLNDBN not specified Trimethylaminuria
Reversed 0
HGVS NC_000001.10:g.171083174C>T
CLNSRC
CLNACC RCV000249666.1, RCV000296336.1,