Have questions? Visit https://www.reddit.com/r/SNPedia

rs1126442

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1126442(A;A)
Make rs1126442(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137156924
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1126442
ebirs1126442
HLIrs1126442
Exacrs1126442
Varsomers1126442
Maprs1126442
PheGenIrs1126442
hapmaprs1126442
1000 genomesrs1126442
hgdprs1126442
ensemblrs1126442
gopubmedrs1126442
geneviewrs1126442
scholarrs1126442
googlers1126442
pharmgkbrs1126442
gwascentralrs1126442
openSNPrs1126442
23andMers1126442
23andMe allrs1126442
SNP Nexus

SNPshotrs1126442
SNPdbers1126442
MSV3drs1126442
GWAS Ctlgrs1126442
GMAF0.1616
Max Magnitude0

[PMID 23880023] Genetic variation of GRIN1 confers vulnerability to methamphetamine-dependent psychosis in a Thai population

ClinVar
Risk rs1126442(A;A)
Alt rs1126442(A;A)
Reference rs1126442(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene GRIN1
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.140051376G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000117172.2,