Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064797027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position137162681
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1064797027
dbSNP (old)rs1064797027
ClinGenrs1064797027
ebirs1064797027
HLIrs1064797027
Exacrs1064797027
Gnomadrs1064797027
Varsomers1064797027
Maprs1064797027
PheGenIrs1064797027
Biobankrs1064797027
1000 genomesrs1064797027
hgdprs1064797027
ensemblrs1064797027
gopubmedrs1064797027
geneviewrs1064797027
scholarrs1064797027
googlers1064797027
pharmgkbrs1064797027
gwascentralrs1064797027
openSNPrs1064797027
23andMers1064797027
23andMe allrs1064797027
SNPshotrs1064797027
SNPdbers1064797027
MSV3drs1064797027
GWAS Ctlgrs1064797027
Max Magnitude0
ClinVar
Risk rs1064797027(T;T)
Alt rs1064797027(T;T)
Reference Rs1064797027(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140057133C>T
CLNSRC
CLNACC RCV000486169.1,