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rs121908335

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908335(C;T)
Make rs121908335(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position86699324
GeneLDB3
is asnp
is mentioned by
dbSNPrs121908335
ebirs121908335
HLIrs121908335
Exacrs121908335
Varsomers121908335
Maprs121908335
PheGenIrs121908335
hapmaprs121908335
1000 genomesrs121908335
hgdprs121908335
ensemblrs121908335
gopubmedrs121908335
geneviewrs121908335
scholarrs121908335
googlers121908335
pharmgkbrs121908335
gwascentralrs121908335
openSNPrs121908335
23andMers121908335
23andMe allrs121908335
SNP Nexus

SNPshotrs121908335
SNPdbers121908335
MSV3drs121908335
GWAS Ctlgrs121908335
Max Magnitude0
OMIM605906
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908335(T;T)
Alt rs121908335(T;T)
Reference rs121908335(C;C)
Significance Pathogenic
Disease Myofibrillar myopathy not specified
Variation info
Gene LDB3
CLNDBN Myofibrillar myopathy, ZASP-related not specified
Reversed 0
HGVS NC_000010.10:g.88459081C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004994.3, RCV000154745.1,