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rs797044925

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044925(A;A)
Make rs797044925(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137163668
GeneGRIN1
is asnp
is mentioned by
dbSNPrs797044925
ebirs797044925
HLIrs797044925
Exacrs797044925
Varsomers797044925
Maprs797044925
PheGenIrs797044925
hapmaprs797044925
1000 genomesrs797044925
hgdprs797044925
ensemblrs797044925
gopubmedrs797044925
geneviewrs797044925
scholarrs797044925
googlers797044925
pharmgkbrs797044925
gwascentralrs797044925
openSNPrs797044925
23andMers797044925
23andMe allrs797044925
SNP Nexus

SNPshotrs797044925
SNPdbers797044925
MSV3drs797044925
GWAS Ctlgrs797044925
Max Magnitude0
ClinVar
Risk rs797044925(A;A)
Alt rs797044925(A;A)
Reference rs797044925(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GRIN1
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000009.11:g.140058120G>A
CLNSRC
CLNACC RCV000190763.1,