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rs375681722

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs375681722(C;T)
Make rs375681722(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position78702289
GeneTENM4
is asnp
is mentioned by
dbSNPrs375681722
ebirs375681722
HLIrs375681722
Exacrs375681722
Varsomers375681722
Maprs375681722
PheGenIrs375681722
hapmaprs375681722
1000 genomesrs375681722
hgdprs375681722
ensemblrs375681722
gopubmedrs375681722
geneviewrs375681722
scholarrs375681722
googlers375681722
pharmgkbrs375681722
gwascentralrs375681722
openSNPrs375681722
23andMers375681722
23andMe allrs375681722
SNP Nexus

SNPshotrs375681722
SNPdbers375681722
MSV3drs375681722
GWAS Ctlgrs375681722
Max Magnitude0
ClinVar
Risk rs375681722(T;T)
Alt rs375681722(T;T)
Reference rs375681722(C;C)
Significance Pathogenic
Disease Tremor
Variation info
Gene TENM4
CLNDBN Tremor, hereditary essential, 5
Reversed 0
HGVS NC_000011.9:g.78413334C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203527.1,