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rs754639936

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754639936(C;G)
Make rs754639936(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position72408038
GeneMICU1
is asnp
is mentioned by
dbSNPrs754639936
ebirs754639936
HLIrs754639936
Exacrs754639936
Varsomers754639936
Maprs754639936
PheGenIrs754639936
hapmaprs754639936
1000 genomesrs754639936
hgdprs754639936
ensemblrs754639936
gopubmedrs754639936
geneviewrs754639936
scholarrs754639936
googlers754639936
pharmgkbrs754639936
gwascentralrs754639936
openSNPrs754639936
23andMers754639936
23andMe allrs754639936
SNP Nexus

SNPshotrs754639936
SNPdbers754639936
MSV3drs754639936
GWAS Ctlgrs754639936
Max Magnitude0
ClinVar
Risk rs754639936(G;G)
Alt rs754639936(G;G)
Reference rs754639936(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.74167796C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000087303.3,