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rs1060500046

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060500046(A;A)
Make rs1060500046(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position137162649
GeneGRIN1
is asnp
is mentioned by
dbSNPrs1060500046
dbSNP (old)rs1060500046
ClinGenrs1060500046
ebirs1060500046
HLIrs1060500046
Exacrs1060500046
Gnomadrs1060500046
Varsomers1060500046
Maprs1060500046
PheGenIrs1060500046
Biobankrs1060500046
1000 genomesrs1060500046
hgdprs1060500046
ensemblrs1060500046
gopubmedrs1060500046
geneviewrs1060500046
scholarrs1060500046
googlers1060500046
pharmgkbrs1060500046
gwascentralrs1060500046
openSNPrs1060500046
23andMers1060500046
23andMe allrs1060500046
SNPshotrs1060500046
SNPdbers1060500046
MSV3drs1060500046
GWAS Ctlgrs1060500046
Max Magnitude0
ClinVar
Risk rs1060500046(A;A)
Alt rs1060500046(A;A)
Reference Rs1060500046(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene GRIN1
CLNDBN Mental retardation, autosomal dominant 8
Reversed 0
HGVS NC_000009.11:g.140057101G>A
CLNSRC
CLNACC RCV000473483.1,