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

rs1064792865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome22
Position50527716
GeneSCO2, TYMP
is asnp
is mentioned by
dbSNPrs1064792865
dbSNP (old)rs1064792865
ClinGenrs1064792865
ebirs1064792865
HLIrs1064792865
Exacrs1064792865
Gnomadrs1064792865
Varsomers1064792865
LitVarrs1064792865
Maprs1064792865
PheGenIrs1064792865
Biobankrs1064792865
1000 genomesrs1064792865
hgdprs1064792865
ensemblrs1064792865
gopubmedrs1064792865
geneviewrs1064792865
scholarrs1064792865
googlers1064792865
pharmgkbrs1064792865
gwascentralrs1064792865
openSNPrs1064792865
23andMers1064792865
23andMe allrs1064792865
SNPshotrs1064792865
SNPdbers1064792865
MSV3drs1064792865
GWAS Ctlgrs1064792865
Max Magnitude0
ClinVar
Risk rs1064792865(G;G)
Alt rs1064792865(G;G)
Reference Rs1064792865(T;T)
Significance Pathogenic
Disease Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Variation info
Gene TYMP SCO2
CLNDBN Mitochondrial DNA depletion syndrome 1 (MNGIE type)
Reversed 1
HGVS NC_000022.10:g.50966145A>C
CLNSRC
CLNACC RCV000208685.1,