Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064792879

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome22
Position50525999
GeneSCO2, TYMP
is asnp
is mentioned by
dbSNPrs1064792879
dbSNP (old)rs1064792879
ClinGenrs1064792879
ebirs1064792879
HLIrs1064792879
Exacrs1064792879
Gnomadrs1064792879
Varsomers1064792879
Maprs1064792879
PheGenIrs1064792879
Biobankrs1064792879
1000 genomesrs1064792879
hgdprs1064792879
ensemblrs1064792879
gopubmedrs1064792879
geneviewrs1064792879
scholarrs1064792879
googlers1064792879
pharmgkbrs1064792879
gwascentralrs1064792879
openSNPrs1064792879
23andMers1064792879
23andMe allrs1064792879
SNPshotrs1064792879
SNPdbers1064792879
MSV3drs1064792879
GWAS Ctlgrs1064792879
Max Magnitude0
ClinVar
Risk rs1064792879(A;A)
Alt rs1064792879(A;A)
Reference Rs1064792879(T;T)
Significance Pathogenic
Disease Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Variation info
Gene SCO2 TYMP
CLNDBN Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Reversed 1
HGVS NC_000022.10:g.50964428A>T
CLNSRC
CLNACC RCV000208650.1,