rs587777317

Orientation

plus

Stabilized

plus

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

Make rs587777317(A;A)

Make rs587777317(A;T)

Reference

GRCh38 38.1/142

Chromosome

X

Position

41218440

Gene

USP9X

is a	snp
is	mentioned by
dbSNP	rs587777317
dbSNP (classic)	rs587777317
ClinGen	rs587777317
ebi	rs587777317
HLI	rs587777317
Exac	rs587777317
Gnomad	rs587777317
Varsome	rs587777317
LitVar	rs587777317
Map	rs587777317
PheGenI	rs587777317
Biobank	rs587777317
1000 genomes	rs587777317
hgdp	rs587777317
ensembl	rs587777317
geneview	rs587777317
scholar	rs587777317
google	rs587777317
pharmgkb	rs587777317
gwascentral	rs587777317
openSNP	rs587777317
23andMe	rs587777317
SNPshot	rs587777317
SNPdbe	rs587777317
MSV3d	rs587777317
GWAS Ctlg	rs587777317

Max Magnitude

0

ClinVar
Risk	rs587777317(A;A)
Alt	rs587777317(A;A)
Reference	Rs587777317(T;T)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	USP9X
CLNDBN	Mental retardation, X-linked 99
Reversed	0
HGVS	NC_000023.10:g.41077693T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000114949.2,