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rs1057520649

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520649(G;T)
Make rs1057520649(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position171114038
GeneFMO3
is asnp
is mentioned by
dbSNPrs1057520649
dbSNP (old)rs1057520649
ClinGenrs1057520649
ebirs1057520649
HLIrs1057520649
Exacrs1057520649
Gnomadrs1057520649
Varsomers1057520649
LitVarrs1057520649
Maprs1057520649
PheGenIrs1057520649
Biobankrs1057520649
1000 genomesrs1057520649
hgdprs1057520649
ensemblrs1057520649
gopubmedrs1057520649
geneviewrs1057520649
scholarrs1057520649
googlers1057520649
pharmgkbrs1057520649
gwascentralrs1057520649
openSNPrs1057520649
23andMers1057520649
23andMe allrs1057520649
SNPshotrs1057520649
SNPdbers1057520649
MSV3drs1057520649
GWAS Ctlgrs1057520649
Max Magnitude0
ClinVar
Risk rs1057520649(T;T)
Alt rs1057520649(T;T)
Reference Rs1057520649(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FMO3
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.171083178G>T
CLNSRC
CLNACC RCV000439141.1,