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rs28363581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28363581(C;C)
Make rs28363581(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position171114258
GeneFMO3
is asnp
is mentioned by
dbSNPrs28363581
dbSNP (old)rs28363581
ClinGenrs28363581
ebirs28363581
HLIrs28363581
Exacrs28363581
Gnomadrs28363581
Varsomers28363581
Maprs28363581
PheGenIrs28363581
Biobankrs28363581
1000 genomesrs28363581
hgdprs28363581
ensemblrs28363581
gopubmedrs28363581
geneviewrs28363581
scholarrs28363581
googlers28363581
pharmgkbrs28363581
gwascentralrs28363581
openSNPrs28363581
23andMers28363581
23andMe allrs28363581
SNP Nexus

SNPshotrs28363581
SNPdbers28363581
MSV3drs28363581
GWAS Ctlgrs28363581
GMAF0.001377
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs28363581(C;C)
Alt rs28363581(C;C)
Reference Rs28363581(T;T)
Significance Other
Disease Trimethylaminuria
Variation info
Gene FMO3
CLNDBN Trimethylaminuria
Reversed 0
HGVS NC_000001.10:g.171083398T>C
CLNSRC UniProtKB (protein)
CLNACC RCV000020652.1,