rs869312865

Orientation

plus

Stabilized

plus

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

Make rs869312865(C;C)

Make rs869312865(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

137156676

Gene	GRIN1, LOC105376328

is a	snp
is	mentioned by
dbSNP	rs869312865
dbSNP (classic)	rs869312865
ClinGen	rs869312865
ebi	rs869312865
HLI	rs869312865
Exac	rs869312865
Gnomad	rs869312865
Varsome	rs869312865
LitVar	rs869312865
Map	rs869312865
PheGenI	rs869312865
Biobank	rs869312865
1000 genomes	rs869312865
hgdp	rs869312865
ensembl	rs869312865
geneview	rs869312865
scholar	rs869312865
google	rs869312865
pharmgkb	rs869312865
gwascentral	rs869312865
openSNP	rs869312865
23andMe	rs869312865
SNPshot	rs869312865
SNPdbe	rs869312865
MSV3d	rs869312865
GWAS Ctlg	rs869312865

Max Magnitude

0

ClinVar
Risk	rs869312865(C;C)
Alt	rs869312865(C;C)
Reference	Rs869312865(G;G)
Significance	Probable-Pathogenic
Disease	Mental retardation
Variation	info
Gene	GRIN1
CLNDBN	Mental retardation, autosomal dominant 8
Reversed	0
HGVS	NC_000009.11:g.140051128G>C
CLNSRC
CLNACC	RCV000210389.1,