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rs8057394

From SNPedia

Orientationplus
Stabilizedplus
Make rs8057394(C;C)
Make rs8057394(C;G)
Make rs8057394(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position10021631
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs8057394
ebirs8057394
HLIrs8057394
Exacrs8057394
Varsomers8057394
Maprs8057394
PheGenIrs8057394
hapmaprs8057394
1000 genomesrs8057394
hgdprs8057394
ensemblrs8057394
gopubmedrs8057394
geneviewrs8057394
scholarrs8057394
googlers8057394
pharmgkbrs8057394
gwascentralrs8057394
openSNPrs8057394
23andMers8057394
23andMe allrs8057394
SNP Nexus

SNPshotrs8057394
SNPdbers8057394
MSV3drs8057394
GWAS Ctlgrs8057394
GMAF0.41
Max Magnitude
? (C;C) (C;G) (G;G) 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.