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rs796052891

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052891(A;G)
Make rs796052891(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320907
GenePOLG
is asnp
is mentioned by
dbSNPrs796052891
ebirs796052891
HLIrs796052891
Exacrs796052891
Varsomers796052891
Maprs796052891
PheGenIrs796052891
hapmaprs796052891
1000 genomesrs796052891
hgdprs796052891
ensemblrs796052891
gopubmedrs796052891
geneviewrs796052891
scholarrs796052891
googlers796052891
pharmgkbrs796052891
gwascentralrs796052891
openSNPrs796052891
23andMers796052891
23andMe allrs796052891
SNP Nexus

SNPshotrs796052891
SNPdbers796052891
MSV3drs796052891
GWAS Ctlgrs796052891
Max Magnitude0
ClinVar
Risk rs796052891(G;G)
Alt rs796052891(G;G)
Reference rs796052891(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89864138T>C
CLNSRC
CLNACC RCV000188590.1,