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rs199476140

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs199476140(-;-)
Make rs199476140(-;A)
Make rs199476140(A;A)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position4366
GeneTBC1D16
is asnp
is mentioned by
dbSNPrs199476140
ebirs199476140
HLIrs199476140
Exacrs199476140
Varsomers199476140
Maprs199476140
PheGenIrs199476140
hapmaprs199476140
1000 genomesrs199476140
hgdprs199476140
ensemblrs199476140
gopubmedrs199476140
geneviewrs199476140
scholarrs199476140
googlers199476140
pharmgkbrs199476140
gwascentralrs199476140
openSNPrs199476140
23andMers199476140
23andMe allrs199476140
SNP Nexus

SNPshotrs199476140
SNPdbers199476140
MSV3drs199476140
GWAS Ctlgrs199476140
Max Magnitude0
ClinVar
Risk rs199476140(A;A)
Alt rs199476140(A;A)
Reference rs199476140(;)
Significance Pathogenic
Disease Myopathy
Variation info
Gene
CLNDBN Myopathy
Reversed 0
HGVS NC_012920.1:m.4369dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010238.2,