rs587777361

Orientation

plus

Stabilized

plus

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

Make rs587777361(C;C)

Make rs587777361(C;G)

Reference

GRCh38 38.1/142

Chromosome

X

Position

123427951

Gene

GRIA3

is a	snp
is	mentioned by
dbSNP	rs587777361
dbSNP (classic)	rs587777361
ClinGen	rs587777361
ebi	rs587777361
HLI	rs587777361
Exac	rs587777361
Gnomad	rs587777361
Varsome	rs587777361
LitVar	rs587777361
Map	rs587777361
PheGenI	rs587777361
Biobank	rs587777361
1000 genomes	rs587777361
hgdp	rs587777361
ensembl	rs587777361
geneview	rs587777361
scholar	rs587777361
google	rs587777361
pharmgkb	rs587777361
gwascentral	rs587777361
openSNP	rs587777361
23andMe	rs587777361
SNPshot	rs587777361
SNPdbe	rs587777361
MSV3d	rs587777361
GWAS Ctlg	rs587777361

Max Magnitude

0

ClinVar
Risk	rs587777361(C;C)
Alt	rs587777361(C;C)
Reference	Rs587777361(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIA3
CLNDBN	Mental retardation, X-linked, syndromic, wu type
Reversed	0
HGVS	NC_000023.10:g.122561802G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000115024.2,