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rs796052884

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052884(C;C)
Make rs796052884(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89323403
GenePOLG
is asnp
is mentioned by
dbSNPrs796052884
ebirs796052884
HLIrs796052884
Exacrs796052884
Varsomers796052884
Maprs796052884
PheGenIrs796052884
hapmaprs796052884
1000 genomesrs796052884
hgdprs796052884
ensemblrs796052884
gopubmedrs796052884
geneviewrs796052884
scholarrs796052884
googlers796052884
pharmgkbrs796052884
gwascentralrs796052884
openSNPrs796052884
23andMers796052884
23andMe allrs796052884
SNP Nexus

SNPshotrs796052884
SNPdbers796052884
MSV3drs796052884
GWAS Ctlgrs796052884
Max Magnitude0
ClinVar
Risk rs796052884(C;C)
Alt rs796052884(C;C)
Reference rs796052884(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89866634C>G
CLNSRC
CLNACC RCV000188569.1,