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rs82334

From SNPedia

Orientationplus
Stabilizedplus
Make rs82334(A;A)
Make rs82334(A;C)
Make rs82334(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position3223644
GeneHTT
is asnp
is mentioned by
dbSNPrs82334
ebirs82334
HLIrs82334
Exacrs82334
Varsomers82334
Maprs82334
PheGenIrs82334
hapmaprs82334
1000 genomesrs82334
hgdprs82334
ensemblrs82334
gopubmedrs82334
geneviewrs82334
scholarrs82334
googlers82334
pharmgkbrs82334
gwascentralrs82334
openSNPrs82334
23andMers82334
23andMe allrs82334
SNP Nexus

SNPshotrs82334
SNPdbers82334
MSV3drs82334
GWAS Ctlgrs82334
GMAF0.3108
Max Magnitude
OMIM143100
DescHUNTINGTON DISEASE; HD
Variant
Relatedalso


[PMID 15832309] Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.