Rs111033574

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Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033574(A;A)
Make rs111033574(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position100989822
GeneC10orf2
is asnp
is mentioned by
dbSNPrs111033574
PheGenIrs111033574
nextbiors111033574
hapmaprs111033574
1000 genomesrs111033574
hgdprs111033574
ensemblrs111033574
gopubmedrs111033574
geneviewrs111033574
scholarrs111033574
googlers111033574
pharmgkbrs111033574
gwascentralrs111033574
openSNPrs111033574
23andMers111033574
23andMe allrs111033574
SNP Nexus

SNPshotrs111033574
SNPdbers111033574
MSV3drs111033574
Max Magnitude0
OMIM606075
Desc
Variant0004
Relatedalso
ClinVar
Risk rs111033574(T;T)
Alt rs111033574(T;T)
Reference rs111033574(G;G)
Significance Pathogenic
Disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
Variation info
Gene C10orf2
CLNDBN Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
Reversed 0
HGVS NC_000010.10:g.102749579G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004882.1,