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rs796065312

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796065312(C;T)
Make rs796065312(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position43683572
GeneMAOA
is asnp
is mentioned by
dbSNPrs796065312
ebirs796065312
HLIrs796065312
Exacrs796065312
Varsomers796065312
Maprs796065312
PheGenIrs796065312
hapmaprs796065312
1000 genomesrs796065312
hgdprs796065312
ensemblrs796065312
gopubmedrs796065312
geneviewrs796065312
scholarrs796065312
googlers796065312
pharmgkbrs796065312
gwascentralrs796065312
openSNPrs796065312
23andMers796065312
23andMe allrs796065312
SNP Nexus

SNPshotrs796065312
SNPdbers796065312
MSV3drs796065312
GWAS Ctlgrs796065312
Max Magnitude0
ClinVar
Risk rs796065312(T;T)
Alt rs796065312(T;T)
Reference rs796065312(C;C)
Significance Pathogenic
Disease Monoamine oxidase A deficiency
Variation info
Gene MAOA
CLNDBN Monoamine oxidase A deficiency
Reversed 0
HGVS NC_000023.10:g.43542820C>T
CLNSRC
CLNACC RCV000190424.1,