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rs768653086

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768653086(C;T)
Make rs768653086(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320917
GenePOLG
is asnp
is mentioned by
dbSNPrs768653086
ebirs768653086
HLIrs768653086
Exacrs768653086
Varsomers768653086
Maprs768653086
PheGenIrs768653086
hapmaprs768653086
1000 genomesrs768653086
hgdprs768653086
ensemblrs768653086
gopubmedrs768653086
geneviewrs768653086
scholarrs768653086
googlers768653086
pharmgkbrs768653086
gwascentralrs768653086
openSNPrs768653086
23andMers768653086
23andMe allrs768653086
SNP Nexus

SNPshotrs768653086
SNPdbers768653086
MSV3drs768653086
GWAS Ctlgrs768653086
Max Magnitude0
ClinVar
Risk rs768653086(T;T)
Alt rs768653086(T;T)
Reference rs768653086(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89864148C>T
CLNSRC
CLNACC RCV000188589.2,