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rs3774729

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3774729(A;A)
Make rs3774729(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position63996406
GeneATXN7
is asnp
is mentioned by
dbSNPrs3774729
ebirs3774729
HLIrs3774729
Exacrs3774729
Varsomers3774729
Maprs3774729
PheGenIrs3774729
hapmaprs3774729
1000 genomesrs3774729
hgdprs3774729
ensemblrs3774729
gopubmedrs3774729
geneviewrs3774729
scholarrs3774729
googlers3774729
pharmgkbrs3774729
gwascentralrs3774729
openSNPrs3774729
23andMers3774729
23andMe allrs3774729
SNP Nexus

SNPshotrs3774729
SNPdbers3774729
MSV3drs3774729
GWAS Ctlgrs3774729
GMAF0.4362
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 23100044] Genetic Variation in Ataxia Gene ATXN7 Influences Cerebellar Grey Matter Volume in Healthy Adults


ClinVar
Risk rs3774729(A;A)
Alt rs3774729(A;A)
Reference rs3774729(G;G)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene ATXN7
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.63982082G>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000116488.2,