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rs587777457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777457(G;T)
Make rs587777457(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position43731695
GeneMAOA
is asnp
is mentioned by
dbSNPrs587777457
ebirs587777457
HLIrs587777457
Exacrs587777457
Varsomers587777457
Maprs587777457
PheGenIrs587777457
hapmaprs587777457
1000 genomesrs587777457
hgdprs587777457
ensemblrs587777457
gopubmedrs587777457
geneviewrs587777457
scholarrs587777457
googlers587777457
pharmgkbrs587777457
gwascentralrs587777457
openSNPrs587777457
23andMers587777457
23andMe allrs587777457
SNP Nexus

SNPshotrs587777457
SNPdbers587777457
MSV3drs587777457
GWAS Ctlgrs587777457
Max Magnitude0
ClinVar
Risk rs587777457(T;T)
Alt rs587777457(T;T)
Reference rs587777457(G;G)
Significance Pathogenic
Disease Monoamine oxidase A deficiency
Variation info
Gene MAOA
CLNDBN Monoamine oxidase A deficiency
Reversed 0
HGVS NC_000023.10:g.43590942G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128399.3,