rs587777457

Orientation

plus

Stabilized

plus

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

Make rs587777457(G;T)

Make rs587777457(T;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

43731695

Gene

MAOA

is a	snp
is	mentioned by
dbSNP	rs587777457
dbSNP (classic)	rs587777457
ClinGen	rs587777457
ebi	rs587777457
HLI	rs587777457
Exac	rs587777457
Gnomad	rs587777457
Varsome	rs587777457
LitVar	rs587777457
Map	rs587777457
PheGenI	rs587777457
Biobank	rs587777457
1000 genomes	rs587777457
hgdp	rs587777457
ensembl	rs587777457
geneview	rs587777457
scholar	rs587777457
google	rs587777457
pharmgkb	rs587777457
gwascentral	rs587777457
openSNP	rs587777457
23andMe	rs587777457
SNPshot	rs587777457
SNPdbe	rs587777457
MSV3d	rs587777457
GWAS Ctlg	rs587777457

Max Magnitude

0

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 UniProtKB (protein)
CLNACC	RCV000128399.3,