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rs3832024

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs3832024(-;-)
Make rs3832024(-;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position171108185
GeneFMO3
is asnp
is mentioned by
dbSNPrs3832024
dbSNP (classic)rs3832024
ClinGenrs3832024
ebirs3832024
HLIrs3832024
Exacrs3832024
Gnomadrs3832024
Varsomers3832024
LitVarrs3832024
Maprs3832024
PheGenIrs3832024
Biobankrs3832024
1000 genomesrs3832024
hgdprs3832024
ensemblrs3832024
geneviewrs3832024
scholarrs3832024
googlers3832024
pharmgkbrs3832024
gwascentralrs3832024
openSNPrs3832024
23andMers3832024
SNPshotrs3832024
SNPdbers3832024
MSV3drs3832024
GWAS Ctlgrs3832024
Max Magnitude0
ClinVar
Risk rs3832024(-;-)
Alt rs3832024(-;-)
Reference Rs3832024(TG;TG)
Significance Pathogenic
Disease Trimethylaminuria
Variation info
Gene FMO3
CLNDBN Trimethylaminuria
Reversed 0
HGVS NC_000001.10:g.171077326_171077327delTG
CLNSRC
CLNACC RCV000490504.1,