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rs793888526

From SNPedia

Orientationplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs793888526(-;-)
Make rs793888526(-;AGA)
Make rs793888526(AGA;AGA)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position2430489
GeneTGM6
is asnp
is mentioned by
dbSNPrs793888526
ebirs793888526
HLIrs793888526
Exacrs793888526
Varsomers793888526
Maprs793888526
PheGenIrs793888526
hapmaprs793888526
1000 genomesrs793888526
hgdprs793888526
ensemblrs793888526
gopubmedrs793888526
geneviewrs793888526
scholarrs793888526
googlers793888526
pharmgkbrs793888526
gwascentralrs793888526
openSNPrs793888526
23andMers793888526
23andMe allrs793888526
SNP Nexus

SNPshotrs793888526
SNPdbers793888526
MSV3drs793888526
GWAS Ctlgrs793888526
Max Magnitude0
ClinVar
Risk rs793888526(;)
Alt rs793888526(;)
Reference rs793888526(AAG;AAG)
Significance Pathogenic
Disease Spinocerebellar ataxia 35
Variation info
Gene TGM6
CLNDBN Spinocerebellar ataxia 35
Reversed 0
HGVS NC_000020.10:g.2411135_2411137delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000170475.3,