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rs747838255

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747838255(A;A)
Make rs747838255(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position9840746
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs747838255
ebirs747838255
HLIrs747838255
Exacrs747838255
Varsomers747838255
Maprs747838255
PheGenIrs747838255
hapmaprs747838255
1000 genomesrs747838255
hgdprs747838255
ensemblrs747838255
gopubmedrs747838255
geneviewrs747838255
scholarrs747838255
googlers747838255
pharmgkbrs747838255
gwascentralrs747838255
openSNPrs747838255
23andMers747838255
23andMe allrs747838255
SNP Nexus

SNPshotrs747838255
SNPdbers747838255
MSV3drs747838255
GWAS Ctlgrs747838255
Max Magnitude0
ClinVar
Risk rs747838255(A;A)
Alt rs747838255(A;A)
Reference rs747838255(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.9934603G>A
CLNSRC
CLNACC RCV000187674.1,