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rs1064795337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome9
Position137162063
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1064795337
dbSNP (classic)rs1064795337
ClinGenrs1064795337
ebirs1064795337
HLIrs1064795337
Exacrs1064795337
Gnomadrs1064795337
Varsomers1064795337
LitVarrs1064795337
Maprs1064795337
PheGenIrs1064795337
Biobankrs1064795337
1000 genomesrs1064795337
hgdprs1064795337
ensemblrs1064795337
geneviewrs1064795337
scholarrs1064795337
googlers1064795337
pharmgkbrs1064795337
gwascentralrs1064795337
openSNPrs1064795337
23andMers1064795337
23andMe allrs1064795337
SNPshotrs1064795337
SNPdbers1064795337
MSV3drs1064795337
GWAS Ctlgrs1064795337
Max Magnitude0
ClinVar
Risk rs1064795337(G;G)
Alt rs1064795337(G;G)
Reference Rs1064795337(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140056515A>G
CLNSRC
CLNACC RCV000484871.1,