rs1805477

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(T;T)	0	common in clinvar

Make rs1805477(C;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

13561795

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs1805477
dbSNP (classic)	rs1805477
ClinGen	rs1805477
ebi	rs1805477
HLI	rs1805477
Exac	rs1805477
Gnomad	rs1805477
Varsome	rs1805477
LitVar	rs1805477
Map	rs1805477
PheGenI	rs1805477
Biobank	rs1805477
1000 genomes	rs1805477
hgdp	rs1805477
ensembl	rs1805477
geneview	rs1805477
scholar	rs1805477
google	rs1805477
pharmgkb	rs1805477
gwascentral	rs1805477
openSNP	rs1805477
23andMe	rs1805477
SNPshot	rs1805477
SNPdbe	rs1805477
MSV3d	rs1805477
GWAS Ctlg	rs1805477

GMAF

0.07943

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 22433450] Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder

ClinVar
Risk	Rs1805477(C;C) rs1805477(G;G)
Alt	Rs1805477(C;C) rs1805477(G;G)
Reference	Rs1805477(T;T)
Significance	Probable-non-pathogenic
Disease	Intellectual Disability
Variation	info
Gene	GRIN2B
CLNDBN	Intellectual Disability, Dominant
Reversed	0
HGVS	NC_000012.11:g.13714729T>C
CLNSRC
CLNACC	RCV000389607.1,