Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064795647

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position9769019
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1064795647
dbSNP (classic)rs1064795647
ClinGenrs1064795647
ebirs1064795647
HLIrs1064795647
Exacrs1064795647
Gnomadrs1064795647
Varsomers1064795647
LitVarrs1064795647
Maprs1064795647
PheGenIrs1064795647
Biobankrs1064795647
1000 genomesrs1064795647
hgdprs1064795647
ensemblrs1064795647
geneviewrs1064795647
scholarrs1064795647
googlers1064795647
pharmgkbrs1064795647
gwascentralrs1064795647
openSNPrs1064795647
23andMers1064795647
23andMe allrs1064795647
SNPshotrs1064795647
SNPdbers1064795647
MSV3drs1064795647
GWAS Ctlgrs1064795647
Max Magnitude0
ClinVar
Risk rs1064795647(A;A)
Alt rs1064795647(A;A)
Reference Rs1064795647(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9862876G>T
CLNSRC
CLNACC RCV000479794.1,