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rs538881762

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs538881762(C;T)
Make rs538881762(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position78726217
GeneLOC107984422, TENM4
is asnp
is mentioned by
dbSNPrs538881762
dbSNP (old)rs538881762
ClinGenrs538881762
ebirs538881762
HLIrs538881762
Exacrs538881762
Gnomadrs538881762
Varsomers538881762
Maprs538881762
PheGenIrs538881762
Biobankrs538881762
1000 genomesrs538881762
hgdprs538881762
ensemblrs538881762
gopubmedrs538881762
geneviewrs538881762
scholarrs538881762
googlers538881762
pharmgkbrs538881762
gwascentralrs538881762
openSNPrs538881762
23andMers538881762
23andMe allrs538881762
SNP Nexus

SNPshotrs538881762
SNPdbers538881762
MSV3drs538881762
GWAS Ctlgrs538881762
Max Magnitude0
ClinVar
Risk rs538881762(T;T)
Alt rs538881762(T;T)
Reference Rs538881762(C;C)
Significance Pathogenic
Disease Tremor
Variation info
Gene TENM4
CLNDBN Tremor, hereditary essential, 5
Reversed 0
HGVS NC_000011.9:g.78437262C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000203554.1,