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rs362277

From SNPedia

Orientationminus
Stabilizedminus
Make rs362277(A;A)
Make rs362277(A;G)
Make rs362277(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position3217326
GeneHTT
is asnp
is mentioned by
dbSNPrs362277
ebirs362277
HLIrs362277
Exacrs362277
Varsomers362277
Maprs362277
PheGenIrs362277
hapmaprs362277
1000 genomesrs362277
hgdprs362277
ensemblrs362277
gopubmedrs362277
geneviewrs362277
scholarrs362277
googlers362277
pharmgkbrs362277
gwascentralrs362277
openSNPrs362277
23andMers362277
23andMe allrs362277
SNP Nexus

SNPshotrs362277
SNPdbers362277
MSV3drs362277
GWAS Ctlgrs362277
GMAF0.1869
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 22134093] Polymorphisms and noncardioembolic stroke in three case-control studies [PMID 16391835] Late-onset and typical Huntington disease families from Crete have distinct genetic origins.