rs144902457

Orientation

plus

Stabilized

plus

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

Make rs144902457(C;C)

Make rs144902457(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

123253500

Gene

GRIA3

is a	snp
is	mentioned by
dbSNP	rs144902457
dbSNP (classic)	rs144902457
ClinGen	rs144902457
ebi	rs144902457
HLI	rs144902457
Exac	rs144902457
Gnomad	rs144902457
Varsome	rs144902457
LitVar	rs144902457
Map	rs144902457
PheGenI	rs144902457
Biobank	rs144902457
1000 genomes	rs144902457
hgdp	rs144902457
ensembl	rs144902457
geneview	rs144902457
scholar	rs144902457
google	rs144902457
pharmgkb	rs144902457
gwascentral	rs144902457
openSNP	rs144902457
23andMe	rs144902457
SNPshot	rs144902457
SNPdbe	rs144902457
MSV3d	rs144902457
GWAS Ctlg	rs144902457

Max Magnitude

0

ClinVar
Risk	rs144902457(C;C)
Alt	rs144902457(C;C)
Reference	Rs144902457(T;T)
Significance	Probable-non-pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIA3
CLNDBN	Mental retardation, X-linked, syndromic, wu type
Reversed	0
HGVS	NC_000023.10:g.122387351T>C
CLNSRC
CLNACC	RCV000209928.2,