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rs369915689

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369915689(C;T)
Make rs369915689(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position72477173
GeneMICU1
is asnp
is mentioned by
dbSNPrs369915689
ebirs369915689
HLIrs369915689
Exacrs369915689
Varsomers369915689
Maprs369915689
PheGenIrs369915689
hapmaprs369915689
1000 genomesrs369915689
hgdprs369915689
ensemblrs369915689
gopubmedrs369915689
geneviewrs369915689
scholarrs369915689
googlers369915689
pharmgkbrs369915689
gwascentralrs369915689
openSNPrs369915689
23andMers369915689
23andMe allrs369915689
SNP Nexus

SNPshotrs369915689
SNPdbers369915689
MSV3drs369915689
GWAS Ctlgrs369915689
Max Magnitude0
ClinVar
Risk rs369915689(T;T)
Alt rs369915689(T;T)
Reference rs369915689(C;C)
Significance Pathogenic
Disease Myopathy with extrapyramidal signs
Variation info
Gene MICU1
CLNDBN Myopathy with extrapyramidal signs
Reversed 0
HGVS NC_000010.10:g.74236931C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087304.3,