Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312865
rs869312865
GRIN1 ; LOC105376328
0.800 GeneticVariation UNIPROT Novel homozygous missense variant of GRIN1 in two sibs with intellectual disability and autistic features without epilepsy. 28051072

2017
dbSNP: rs869312865
rs869312865
GRIN1 ; LOC105376328
0.800 GeneticVariation UNIPROT Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. 27164704

2016
dbSNP: rs869312865
rs869312865
GRIN1 ; LOC105376328
C 0.800 GeneticVariation CLINVAR

dbSNP: rs1554770667
rs1554770667
GRIN1
T 0.700 GeneticVariation CLINVAR