rs387906635

Orientation

plus

Stabilized

plus

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

Make rs387906635(A;A)

Make rs387906635(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

137162710

Gene

GRIN1

is a	snp
is	mentioned by
dbSNP	rs387906635
dbSNP (classic)	rs387906635
ClinGen	rs387906635
ebi	rs387906635
HLI	rs387906635
Exac	rs387906635
Gnomad	rs387906635
Varsome	rs387906635
LitVar	rs387906635
Map	rs387906635
PheGenI	rs387906635
Biobank	rs387906635
1000 genomes	rs387906635
hgdp	rs387906635
ensembl	rs387906635
geneview	rs387906635
scholar	rs387906635
google	rs387906635
pharmgkb	rs387906635
gwascentral	rs387906635
openSNP	rs387906635
23andMe	rs387906635
SNPshot	rs387906635
SNPdbe	rs387906635
MSV3d	rs387906635
GWAS Ctlg	rs387906635

Max Magnitude

0

ClinVar
Risk	rs387906635(A;A)
Alt	rs387906635(A;A)
Reference	Rs387906635(G;G)
Significance	Pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIN1
CLNDBN	Mental retardation, autosomal dominant 8
Reversed	0
HGVS	NC_000009.11:g.140057162G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000022577.27,