rs876661219

Orientation

minus

Stabilized

minus

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

Make rs876661219(C;C)

Make rs876661219(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

13571891

Gene

GRIN2B

is a	snp
is	mentioned by
dbSNP	rs876661219
dbSNP (classic)	rs876661219
ClinGen	rs876661219
ebi	rs876661219
HLI	rs876661219
Exac	rs876661219
Gnomad	rs876661219
Varsome	rs876661219
LitVar	rs876661219
Map	rs876661219
PheGenI	rs876661219
Biobank	rs876661219
1000 genomes	rs876661219
hgdp	rs876661219
ensembl	rs876661219
geneview	rs876661219
scholar	rs876661219
google	rs876661219
pharmgkb	rs876661219
gwascentral	rs876661219
openSNP	rs876661219
23andMe	rs876661219
SNPshot	rs876661219
SNPdbe	rs876661219
MSV3d	rs876661219
GWAS Ctlg	rs876661219

Max Magnitude

0

ClinVar
Risk	rs876661219(C;C)
Alt	rs876661219(C;C)
Reference	Rs876661219(T;T)
Significance	Probable-Pathogenic
Disease	not provided Ataxia intellectual deficiency
Variation	info
Gene	GRIN2B
CLNDBN	not provided Ataxia intellectual deficiency
Reversed	1
HGVS	NC_000012.11:g.13724825A>G
CLNSRC
CLNACC	RCV000214460.1, RCV000415402.1,