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rs2650427

From SNPedia

Orientationplus
Stabilizedplus
Make rs2650427(C;C)
Make rs2650427(C;T)
Make rs2650427(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position10020701
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs2650427
ebirs2650427
HLIrs2650427
Exacrs2650427
Varsomers2650427
Maprs2650427
PheGenIrs2650427
hapmaprs2650427
1000 genomesrs2650427
hgdprs2650427
ensemblrs2650427
gopubmedrs2650427
geneviewrs2650427
scholarrs2650427
googlers2650427
pharmgkbrs2650427
gwascentralrs2650427
openSNPrs2650427
23andMers2650427
23andMe allrs2650427
SNP Nexus

SNPshotrs2650427
SNPdbers2650427
MSV3drs2650427
GWAS Ctlgrs2650427
GMAF0.4605
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM143100
DescHUNTINGTON DISEASE; HD
Variant
Relatedalso


[PMID 17569088] NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.


[PMID 23644918OA-icon.png] Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.