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rs121908489

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908489(C;T)
Make rs121908489(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position94628303
GeneSGCE
is asnp
is mentioned by
dbSNPrs121908489
ebirs121908489
HLIrs121908489
Exacrs121908489
Varsomers121908489
Maprs121908489
PheGenIrs121908489
hapmaprs121908489
1000 genomesrs121908489
hgdprs121908489
ensemblrs121908489
gopubmedrs121908489
geneviewrs121908489
scholarrs121908489
googlers121908489
pharmgkbrs121908489
gwascentralrs121908489
openSNPrs121908489
23andMers121908489
23andMe allrs121908489
SNP Nexus

SNPshotrs121908489
SNPdbers121908489
MSV3drs121908489
GWAS Ctlgrs121908489
Max Magnitude0
OMIM604149
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908489(T;T)
Alt rs121908489(T;T)
Reference rs121908489(C;C)
Significance Pathogenic
Disease Myoclonic dystonia
Variation info
Gene SGCE
CLNDBN Myoclonic dystonia
Reversed 1
HGVS NC_000007.13:g.94257615G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006124.3,