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rs1064794987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position137142083
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1064794987
dbSNP (old)rs1064794987
ClinGenrs1064794987
ebirs1064794987
HLIrs1064794987
Exacrs1064794987
Gnomadrs1064794987
Varsomers1064794987
Maprs1064794987
PheGenIrs1064794987
Biobankrs1064794987
1000 genomesrs1064794987
hgdprs1064794987
ensemblrs1064794987
gopubmedrs1064794987
geneviewrs1064794987
scholarrs1064794987
googlers1064794987
pharmgkbrs1064794987
gwascentralrs1064794987
openSNPrs1064794987
23andMers1064794987
23andMe allrs1064794987
SNPshotrs1064794987
SNPdbers1064794987
MSV3drs1064794987
GWAS Ctlgrs1064794987
Max Magnitude0
ClinVar
Risk rs1064794987(T;T)
Alt rs1064794987(T;T)
Reference Rs1064794987(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140036535C>T
CLNSRC
CLNACC RCV000484875.1,