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rs606231177

From SNPedia

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Geno Mag Summary
(;) 0 common in clinvar
Make rs606231177(-;-)
Make rs606231177(-;A)
Make rs606231177(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeMT
Position4369
is asnp
is mentioned by
dbSNPrs606231177
ebirs606231177
HLIrs606231177
Exacrs606231177
Varsomers606231177
Maprs606231177
PheGenIrs606231177
hapmaprs606231177
1000 genomesrs606231177
hgdprs606231177
ensemblrs606231177
gopubmedrs606231177
geneviewrs606231177
scholarrs606231177
googlers606231177
pharmgkbrs606231177
gwascentralrs606231177
openSNPrs606231177
23andMers606231177
23andMe allrs606231177
SNP Nexus

SNPshotrs606231177
SNPdbers606231177
MSV3drs606231177
GWAS Ctlgrs606231177
Max Magnitude0
ClinVar
Risk rs606231177(A;A)
Alt rs606231177(A;A)
Reference rs606231177(;)
Significance Pathogenic
Disease Myopathy
Variation info
Gene
CLNDBN Myopathy
Reversed 0
HGVS NC_012920.1:m.4369dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010238.2,