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rs1064795158

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position137162051
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1064795158
dbSNP (old)rs1064795158
ClinGenrs1064795158
ebirs1064795158
HLIrs1064795158
Exacrs1064795158
Gnomadrs1064795158
Varsomers1064795158
LitVarrs1064795158
Maprs1064795158
PheGenIrs1064795158
Biobankrs1064795158
1000 genomesrs1064795158
hgdprs1064795158
ensemblrs1064795158
gopubmedrs1064795158
geneviewrs1064795158
scholarrs1064795158
googlers1064795158
pharmgkbrs1064795158
gwascentralrs1064795158
openSNPrs1064795158
23andMers1064795158
23andMe allrs1064795158
SNPshotrs1064795158
SNPdbers1064795158
MSV3drs1064795158
GWAS Ctlgrs1064795158
Max Magnitude0
ClinVar
Risk rs1064795158(A;A)
Alt rs1064795158(A;A)
Reference Rs1064795158(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140056503C>A
CLNSRC
CLNACC RCV000484949.1,