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rs139590686

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs139590686(G;G)
Make rs139590686(G;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position89321007
GenePOLG
is asnp
is mentioned by
dbSNPrs139590686
dbSNP (old)rs139590686
ClinGenrs139590686
ebirs139590686
HLIrs139590686
Exacrs139590686
Gnomadrs139590686
Varsomers139590686
Maprs139590686
PheGenIrs139590686
Biobankrs139590686
1000 genomesrs139590686
hgdprs139590686
ensemblrs139590686
gopubmedrs139590686
geneviewrs139590686
scholarrs139590686
googlers139590686
pharmgkbrs139590686
gwascentralrs139590686
openSNPrs139590686
23andMers139590686
23andMe allrs139590686
SNPshotrs139590686
SNPdbers139590686
MSV3drs139590686
GWAS Ctlgrs139590686
Max Magnitude0
ClinVar
Risk rs139590686(G;G)
Alt rs139590686(G;G)
Reference Rs139590686(T;T)
Significance Pathogenic
Disease POLG-Related Spectrum Disorders not provided
Variation info
Gene POLG
CLNDBN POLG-Related Spectrum Disorders not provided
Reversed 0
HGVS NC_000015.9:g.89864238T>G
CLNSRC Illumina
CLNACC RCV000306622.1, RCV000321917.2,