rs1057518114

Orientation

plus

Stabilized

plus

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

Make rs1057518114(-;-)

Make rs1057518114(-;CTT)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

41136888

Gene

USP9X

is a	snp
is	mentioned by
dbSNP	rs1057518114
dbSNP (classic)	rs1057518114
ClinGen	rs1057518114
ebi	rs1057518114
HLI	rs1057518114
Exac	rs1057518114
Gnomad	rs1057518114
Varsome	rs1057518114
LitVar	rs1057518114
Map	rs1057518114
PheGenI	rs1057518114
Biobank	rs1057518114
1000 genomes	rs1057518114
hgdp	rs1057518114
ensembl	rs1057518114
geneview	rs1057518114
scholar	rs1057518114
google	rs1057518114
pharmgkb	rs1057518114
gwascentral	rs1057518114
openSNP	rs1057518114
23andMe	rs1057518114
SNPshot	rs1057518114
SNPdbe	rs1057518114
MSV3d	rs1057518114
GWAS Ctlg	rs1057518114

Max Magnitude

0

ClinVar
Risk	rs1057518114(-;-)
Alt	rs1057518114(-;-)
Reference	Rs1057518114(CTT;CTT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	USP9X
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.40996141_40996143delCTT
CLNSRC
CLNACC	RCV000413770.1,