rs1057519007

Orientation

plus

Stabilized

plus

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

Make rs1057519007(-;-)

Make rs1057519007(-;CC)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

41215906

Gene

USP9X

is a	snp
is	mentioned by
dbSNP	rs1057519007
dbSNP (classic)	rs1057519007
ClinGen	rs1057519007
ebi	rs1057519007
HLI	rs1057519007
Exac	rs1057519007
Gnomad	rs1057519007
Varsome	rs1057519007
LitVar	rs1057519007
Map	rs1057519007
PheGenI	rs1057519007
Biobank	rs1057519007
1000 genomes	rs1057519007
hgdp	rs1057519007
ensembl	rs1057519007
geneview	rs1057519007
scholar	rs1057519007
google	rs1057519007
pharmgkb	rs1057519007
gwascentral	rs1057519007
openSNP	rs1057519007
23andMe	rs1057519007
SNPshot	rs1057519007
SNPdbe	rs1057519007
MSV3d	rs1057519007
GWAS Ctlg	rs1057519007

Max Magnitude

0

ClinVar
Risk	rs1057519007(-;-)
Alt	rs1057519007(-;-)
Reference	Rs1057519007(CC;CC)
Significance	Probable-Pathogenic
Disease	Severe intellectual deficiency
Variation	info
Gene	USP9X
CLNDBN	Severe intellectual deficiency
Reversed	0
HGVS	NC_000023.10:g.41075159_41075160delCC
CLNSRC
CLNACC	RCV000415029.1,