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rs397509391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509391(G;T)
Make rs397509391(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position10154602
GeneDNMT1
is asnp
is mentioned by
dbSNPrs397509391
ebirs397509391
HLIrs397509391
Exacrs397509391
Varsomers397509391
Maprs397509391
PheGenIrs397509391
hapmaprs397509391
1000 genomesrs397509391
hgdprs397509391
ensemblrs397509391
gopubmedrs397509391
geneviewrs397509391
scholarrs397509391
googlers397509391
pharmgkbrs397509391
gwascentralrs397509391
openSNPrs397509391
23andMers397509391
23andMe allrs397509391
SNP Nexus

SNPshotrs397509391
SNPdbers397509391
MSV3drs397509391
GWAS Ctlgrs397509391
Max Magnitude0
ClinVar
Risk rs397509391(T;T)
Alt rs397509391(T;T)
Reference rs397509391(G;G)
Significance Pathogenic
Disease Cerebellar ataxia
Variation info
Gene DNMT1
CLNDBN Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant
Reversed 1
HGVS NC_000019.9:g.10265278C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043631.28,