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rs3764028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs3764028(A;A)
Make rs3764028(A;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position13982130
is asnp
is mentioned by
dbSNPrs3764028
ebirs3764028
HLIrs3764028
Exacrs3764028
Varsomers3764028
Maprs3764028
PheGenIrs3764028
hapmaprs3764028
1000 genomesrs3764028
hgdprs3764028
ensemblrs3764028
gopubmedrs3764028
geneviewrs3764028
scholarrs3764028
googlers3764028
pharmgkbrs3764028
gwascentralrs3764028
openSNPrs3764028
23andMers3764028
23andMe allrs3764028
SNP Nexus

SNPshotrs3764028
SNPdbers3764028
MSV3drs3764028
GWAS Ctlgrs3764028
GMAF0.2107
Max Magnitude0
rs3764028 ( -421C/A ) is a SNP in close proximity to GRIN2B (Glutamate [NMDA] receptor subunit epsilon-2).

[PMID 18983893] significant differences in genotype between the North Chinese sporadic Alzheimer's patients (of which there were 362) and controls (of which there were 334). 34.69-39.79% decreased transcriptional activity (per luciferase reporter assay in SH-SY5Y and HeLa cell lines) noted for the C allele versus the A allele

[PMID 25693086] The relationship of TP53 and GRIN2B gene polymorphisms with risk of occurrence and progression of primary open-angle glaucoma in a Polish population