rs1057524248

Orientation

plus

Stabilized

plus

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

Make rs1057524248(C;T)

Make rs1057524248(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

41137011

Gene

USP9X

is a	snp
is	mentioned by
dbSNP	rs1057524248
dbSNP (classic)	rs1057524248
ClinGen	rs1057524248
ebi	rs1057524248
HLI	rs1057524248
Exac	rs1057524248
Gnomad	rs1057524248
Varsome	rs1057524248
LitVar	rs1057524248
Map	rs1057524248
PheGenI	rs1057524248
Biobank	rs1057524248
1000 genomes	rs1057524248
hgdp	rs1057524248
ensembl	rs1057524248
geneview	rs1057524248
scholar	rs1057524248
google	rs1057524248
pharmgkb	rs1057524248
gwascentral	rs1057524248
openSNP	rs1057524248
23andMe	rs1057524248
SNPshot	rs1057524248
SNPdbe	rs1057524248
MSV3d	rs1057524248
GWAS Ctlg	rs1057524248

Max Magnitude

0

ClinVar
Risk	rs1057524248(T;T)
Alt	rs1057524248(T;T)
Reference	Rs1057524248(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	USP9X
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.40996264C>T
CLNSRC
CLNACC	RCV000431532.1,