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rs769983049

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs769983049(C;C)
Make rs769983049(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position171108154
GeneFMO3
is asnp
is mentioned by
dbSNPrs769983049
ebirs769983049
HLIrs769983049
Exacrs769983049
Varsomers769983049
Maprs769983049
PheGenIrs769983049
hapmaprs769983049
1000 genomesrs769983049
hgdprs769983049
ensemblrs769983049
gopubmedrs769983049
geneviewrs769983049
scholarrs769983049
googlers769983049
pharmgkbrs769983049
gwascentralrs769983049
openSNPrs769983049
23andMers769983049
23andMe allrs769983049
SNP Nexus

SNPshotrs769983049
SNPdbers769983049
MSV3drs769983049
GWAS Ctlgrs769983049
Max Magnitude0
ClinVar
Risk rs769983049(C,G;C,G)
Alt rs769983049(C,G;C,G)
Reference rs769983049(T;T)
Significance Pathogenic
Disease Trimethylaminuria
Variation info
Gene FMO3
CLNDBN Trimethylaminuria
Reversed 0
HGVS NC_000001.10:g.171077295T>C
CLNSRC
CLNACC RCV000201278.1,