rs797045026

Orientation

plus

Stabilized

plus

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

Make rs797045026(C;T)

Make rs797045026(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

41345238

Gene

DDX3X

is a	snp
is	mentioned by
dbSNP	rs797045026
dbSNP (classic)	rs797045026
ClinGen	rs797045026
ebi	rs797045026
HLI	rs797045026
Exac	rs797045026
Gnomad	rs797045026
Varsome	rs797045026
LitVar	rs797045026
Map	rs797045026
PheGenI	rs797045026
Biobank	rs797045026
1000 genomes	rs797045026
hgdp	rs797045026
ensembl	rs797045026
geneview	rs797045026
scholar	rs797045026
google	rs797045026
pharmgkb	rs797045026
gwascentral	rs797045026
openSNP	rs797045026
23andMe	rs797045026
SNPshot	rs797045026
SNPdbe	rs797045026
MSV3d	rs797045026
GWAS Ctlg	rs797045026

Max Magnitude

0

ClinVar
Risk	rs797045026(T;T)
Alt	rs797045026(T;T)
Reference	Rs797045026(C;C)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	DDX3X
CLNDBN	Mental retardation, X-linked 102
Reversed	0
HGVS	NC_000023.10:g.41204491C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000190554.2,