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rs1064792860

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome22
Position50529225
GeneTYMP
is asnp
is mentioned by
dbSNPrs1064792860
dbSNP (classic)rs1064792860
ClinGenrs1064792860
ebirs1064792860
HLIrs1064792860
Exacrs1064792860
Gnomadrs1064792860
Varsomers1064792860
LitVarrs1064792860
Maprs1064792860
PheGenIrs1064792860
Biobankrs1064792860
1000 genomesrs1064792860
hgdprs1064792860
ensemblrs1064792860
geneviewrs1064792860
scholarrs1064792860
googlers1064792860
pharmgkbrs1064792860
gwascentralrs1064792860
openSNPrs1064792860
23andMers1064792860
23andMe allrs1064792860
SNPshotrs1064792860
SNPdbers1064792860
MSV3drs1064792860
GWAS Ctlgrs1064792860
Max Magnitude0
ClinVar
Risk rs1064792860(T;T)
Alt rs1064792860(T;T)
Reference Rs1064792860(C;C)
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.50967654G>A
CLNSRC
CLNACC RCV000208694.1,