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rs796052911

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052911(C;C)
Make rs796052911(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89319031
GenePOLG
is asnp
is mentioned by
dbSNPrs796052911
ebirs796052911
HLIrs796052911
Exacrs796052911
Varsomers796052911
Maprs796052911
PheGenIrs796052911
hapmaprs796052911
1000 genomesrs796052911
hgdprs796052911
ensemblrs796052911
gopubmedrs796052911
geneviewrs796052911
scholarrs796052911
googlers796052911
pharmgkbrs796052911
gwascentralrs796052911
openSNPrs796052911
23andMers796052911
23andMe allrs796052911
SNP Nexus

SNPshotrs796052911
SNPdbers796052911
MSV3drs796052911
GWAS Ctlgrs796052911
Max Magnitude0
ClinVar
Risk rs796052911(C;C)
Alt rs796052911(C;C)
Reference rs796052911(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89862262A>G
CLNSRC
CLNACC RCV000188679.1,