rs797045047

Orientation

plus

Stabilized

plus

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

Make rs797045047(C;C)

Make rs797045047(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

137162510

Gene

GRIN1

is a	snp
is	mentioned by
dbSNP	rs797045047
dbSNP (classic)	rs797045047
ClinGen	rs797045047
ebi	rs797045047
HLI	rs797045047
Exac	rs797045047
Gnomad	rs797045047
Varsome	rs797045047
LitVar	rs797045047
Map	rs797045047
PheGenI	rs797045047
Biobank	rs797045047
1000 genomes	rs797045047
hgdp	rs797045047
ensembl	rs797045047
geneview	rs797045047
scholar	rs797045047
google	rs797045047
pharmgkb	rs797045047
gwascentral	rs797045047
openSNP	rs797045047
23andMe	rs797045047
SNPshot	rs797045047
SNPdbe	rs797045047
MSV3d	rs797045047
GWAS Ctlg	rs797045047

Max Magnitude

0

ClinVar
Risk	rs797045047(C;C)
Alt	rs797045047(C;C)
Reference	Rs797045047(G;G)
Significance	Probable-Pathogenic
Disease	Mental retardation not provided
Variation	info
Gene	GRIN1
CLNDBN	Mental retardation, autosomal dominant 8 not provided
Reversed	0
HGVS	NC_000009.11:g.140056962G>C
CLNSRC	Baylor College of Medicine
CLNACC	RCV000191091.1, RCV000479068.1,