rs193302913

Orientation

minus

Stabilized

minus

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

Make rs193302913(-;-)

Make rs193302913(-;CT)

Reference

GRCh38 38.1/142

Chromosome

X

Position

149490411

Gene

IDS

is a	snp
is	mentioned by
dbSNP	rs193302913
dbSNP (classic)	rs193302913
ClinGen	rs193302913
ebi	rs193302913
HLI	rs193302913
Exac	rs193302913
Gnomad	rs193302913
Varsome	rs193302913
LitVar	rs193302913
Map	rs193302913
PheGenI	rs193302913
Biobank	rs193302913
1000 genomes	rs193302913
hgdp	rs193302913
ensembl	rs193302913
geneview	rs193302913
scholar	rs193302913
google	rs193302913
pharmgkb	rs193302913
gwascentral	rs193302913
openSNP	rs193302913
23andMe	rs193302913
SNPshot	rs193302913
SNPdbe	rs193302913
MSV3d	rs193302913
GWAS Ctlg	rs193302913

Max Magnitude

0

ClinVar
Risk	rs193302913(-;-)
Alt	rs193302913(-;-)
Reference	Rs193302913(CT;CT)
Significance	Pathogenic
Disease	Mucopolysaccharidosis
Variation	info
Gene	IDS
CLNDBN	Mucopolysaccharidosis, MPS-II
Reversed	1
HGVS	NC_000023.10:g.148571942_148571943delAG
CLNSRC
CLNACC	RCV000205483.1,