rs878853143

Orientation

plus

Stabilized

plus

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

Make rs878853143(C;G)

Make rs878853143(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

137162209

Gene

GRIN1

is a	snp
is	mentioned by
dbSNP	rs878853143
dbSNP (classic)	rs878853143
ClinGen	rs878853143
ebi	rs878853143
HLI	rs878853143
Exac	rs878853143
Gnomad	rs878853143
Varsome	rs878853143
LitVar	rs878853143
Map	rs878853143
PheGenI	rs878853143
Biobank	rs878853143
1000 genomes	rs878853143
hgdp	rs878853143
ensembl	rs878853143
geneview	rs878853143
scholar	rs878853143
google	rs878853143
pharmgkb	rs878853143
gwascentral	rs878853143
openSNP	rs878853143
23andMe	rs878853143
SNPshot	rs878853143
SNPdbe	rs878853143
MSV3d	rs878853143
GWAS Ctlg	rs878853143

Max Magnitude

0

ClinVar
Risk	rs878853143(G;G) rs878853143(T;T)
Alt	rs878853143(G;G) rs878853143(T;T)
Reference	Rs878853143(C;C)
Significance	Pathogenic
Disease	Intellectual disability not provided
Variation	info
Gene	GRIN1
CLNDBN	Intellectual disability not provided
Reversed	0
HGVS	NC_000009.11:g.140056661C>G; NC_000009.11:g.140056661C>T
CLNSRC
CLNACC	RCV000224047.1, RCV000412873.1,