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rs387907098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387907098(A;G)
Make rs387907098(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position2400435
GeneTGM6
is asnp
is mentioned by
dbSNPrs387907098
ebirs387907098
HLIrs387907098
Exacrs387907098
Varsomers387907098
Maprs387907098
PheGenIrs387907098
hapmaprs387907098
1000 genomesrs387907098
hgdprs387907098
ensemblrs387907098
gopubmedrs387907098
geneviewrs387907098
scholarrs387907098
googlers387907098
pharmgkbrs387907098
gwascentralrs387907098
openSNPrs387907098
23andMers387907098
23andMe allrs387907098
SNP Nexus

SNPshotrs387907098
SNPdbers387907098
MSV3drs387907098
GWAS Ctlgrs387907098
Max Magnitude0
ClinVar
Risk rs387907098(G;G)
Alt rs387907098(G;G)
Reference rs387907098(A;A)
Significance Pathogenic
Disease Spinocerebellar ataxia 35
Variation info
Gene TGM6
CLNDBN Spinocerebellar ataxia 35
Reversed 0
HGVS NC_000020.10:g.2381081A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024081.2,