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rs1064792886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Chromosome22
Position50529289
GeneTYMP
is asnp
is mentioned by
dbSNPrs1064792886
dbSNP (old)rs1064792886
ClinGenrs1064792886
ebirs1064792886
HLIrs1064792886
Exacrs1064792886
Gnomadrs1064792886
Varsomers1064792886
Maprs1064792886
PheGenIrs1064792886
Biobankrs1064792886
1000 genomesrs1064792886
hgdprs1064792886
ensemblrs1064792886
gopubmedrs1064792886
geneviewrs1064792886
scholarrs1064792886
googlers1064792886
pharmgkbrs1064792886
gwascentralrs1064792886
openSNPrs1064792886
23andMers1064792886
23andMe allrs1064792886
SNPshotrs1064792886
SNPdbers1064792886
MSV3drs1064792886
GWAS Ctlgrs1064792886
Max Magnitude0
ClinVar
Risk rs1064792886(-;-)
Alt rs1064792886(-;-)
Reference Rs1064792886(CC;CC)
Significance Pathogenic
Disease Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Variation info
Gene TYMP
CLNDBN Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Reversed 1
HGVS NC_000022.10:g.50967718_50967719delGG
CLNSRC
CLNACC RCV000208656.1,