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rs796052890

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052890(A;A)
Make rs796052890(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320998
GenePOLG
is asnp
is mentioned by
dbSNPrs796052890
ebirs796052890
HLIrs796052890
Exacrs796052890
Varsomers796052890
Maprs796052890
PheGenIrs796052890
hapmaprs796052890
1000 genomesrs796052890
hgdprs796052890
ensemblrs796052890
gopubmedrs796052890
geneviewrs796052890
scholarrs796052890
googlers796052890
pharmgkbrs796052890
gwascentralrs796052890
openSNPrs796052890
23andMers796052890
23andMe allrs796052890
SNP Nexus

SNPshotrs796052890
SNPdbers796052890
MSV3drs796052890
GWAS Ctlgrs796052890
Max Magnitude0
ClinVar
Risk rs796052890(A;A)
Alt rs796052890(A;A)
Reference rs796052890(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89864229C>T
CLNSRC
CLNACC RCV000188587.1,