rs796065312

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs796065312(C;T)

Make rs796065312(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

43683572

Gene

MAOA

is a	snp
is	mentioned by
dbSNP	rs796065312
dbSNP (classic)	rs796065312
ClinGen	rs796065312
ebi	rs796065312
HLI	rs796065312
Exac	rs796065312
Gnomad	rs796065312
Varsome	rs796065312
LitVar	rs796065312
Map	rs796065312
PheGenI	rs796065312
Biobank	rs796065312
1000 genomes	rs796065312
hgdp	rs796065312
ensembl	rs796065312
geneview	rs796065312
scholar	rs796065312
google	rs796065312
pharmgkb	rs796065312
gwascentral	rs796065312
openSNP	rs796065312
23andMe	rs796065312
SNPshot	rs796065312
SNPdbe	rs796065312
MSV3d	rs796065312
GWAS Ctlg	rs796065312

Max Magnitude

0

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,