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rs796065311

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796065311(-;T)
Make rs796065311(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position43731344
GeneMAOA
is asnp
is mentioned by
dbSNPrs796065311
dbSNP (old)rs796065311
ClinGenrs796065311
ebirs796065311
HLIrs796065311
Exacrs796065311
Gnomadrs796065311
Varsomers796065311
Maprs796065311
PheGenIrs796065311
Biobankrs796065311
1000 genomesrs796065311
hgdprs796065311
ensemblrs796065311
gopubmedrs796065311
geneviewrs796065311
scholarrs796065311
googlers796065311
pharmgkbrs796065311
gwascentralrs796065311
openSNPrs796065311
23andMers796065311
23andMe allrs796065311
SNP Nexus

SNPshotrs796065311
SNPdbers796065311
MSV3drs796065311
GWAS Ctlgrs796065311
Max Magnitude0
ClinVar
Risk rs796065311(T;T)
Alt rs796065311(T;T)
Reference Rs796065311(-;-)
Significance Pathogenic
Disease Monoamine oxidase A deficiency
Variation info
Gene MAOA
CLNDBN Monoamine oxidase A deficiency
Reversed 0
HGVS NC_000023.10:g.43590591_43590592insT
CLNSRC
CLNACC RCV000190423.1,