Have questions? Visit https://www.reddit.com/r/SNPedia

rs199474667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199474667(A;A)
Make rs199474667(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position3249
GeneDDX27
is asnp
is mentioned by
dbSNPrs199474667
ebirs199474667
HLIrs199474667
Exacrs199474667
Varsomers199474667
Maprs199474667
PheGenIrs199474667
hapmaprs199474667
1000 genomesrs199474667
hgdprs199474667
ensemblrs199474667
gopubmedrs199474667
geneviewrs199474667
scholarrs199474667
googlers199474667
pharmgkbrs199474667
gwascentralrs199474667
openSNPrs199474667
23andMers199474667
23andMe allrs199474667
SNP Nexus

SNPshotrs199474667
SNPdbers199474667
MSV3drs199474667
GWAS Ctlgrs199474667
Max Magnitude0
ClinVar
Risk rs199474667(A;A)
Alt rs199474667(A;A)
Reference rs199474667(G;G)
Significance Pathogenic
Disease Kearns Sayre syndrome
Variation info
Gene
CLNDBN Kearns Sayre syndrome
Reversed 0
HGVS NC_012920.1:m.3249G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010222.3,