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rs199474661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199474661(A;G)
Make rs199474661(G;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position3252
GeneDDX27
is asnp
is mentioned by
dbSNPrs199474661
ebirs199474661
HLIrs199474661
Exacrs199474661
Varsomers199474661
Maprs199474661
PheGenIrs199474661
hapmaprs199474661
1000 genomesrs199474661
hgdprs199474661
ensemblrs199474661
gopubmedrs199474661
geneviewrs199474661
scholarrs199474661
googlers199474661
pharmgkbrs199474661
gwascentralrs199474661
openSNPrs199474661
23andMers199474661
23andMe allrs199474661
SNP Nexus

SNPshotrs199474661
SNPdbers199474661
MSV3drs199474661
GWAS Ctlgrs199474661
Max Magnitude0
ClinVar
Risk rs199474661(G;G)
Alt rs199474661(G;G)
Reference rs199474661(A;A)
Significance Pathogenic
Disease Mitochondrial encephalomyopathy
Variation info
Gene
CLNDBN Mitochondrial encephalomyopathy
Reversed 0
HGVS NC_012920.1:m.3252A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010217.2,