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rs201964784

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201964784(C;C)
Make rs201964784(C;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position2417423
GeneTGM6
is asnp
is mentioned by
dbSNPrs201964784
ebirs201964784
HLIrs201964784
Exacrs201964784
Varsomers201964784
Maprs201964784
PheGenIrs201964784
hapmaprs201964784
1000 genomesrs201964784
hgdprs201964784
ensemblrs201964784
gopubmedrs201964784
geneviewrs201964784
scholarrs201964784
googlers201964784
pharmgkbrs201964784
gwascentralrs201964784
openSNPrs201964784
23andMers201964784
23andMe allrs201964784
SNP Nexus

SNPshotrs201964784
SNPdbers201964784
MSV3drs201964784
GWAS Ctlgrs201964784
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs201964784(C;C)
Alt rs201964784(C;C)
Reference rs201964784(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 35
Variation info
Gene TGM6
CLNDBN Spinocerebellar ataxia 35
Reversed 0
HGVS NC_000020.10:g.2398069G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000034865.4,