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rs767709505

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767709505(A;A)
Make rs767709505(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89325683
GenePOLG
is asnp
is mentioned by
dbSNPrs767709505
ebirs767709505
HLIrs767709505
Exacrs767709505
Varsomers767709505
Maprs767709505
PheGenIrs767709505
hapmaprs767709505
1000 genomesrs767709505
hgdprs767709505
ensemblrs767709505
gopubmedrs767709505
geneviewrs767709505
scholarrs767709505
googlers767709505
pharmgkbrs767709505
gwascentralrs767709505
openSNPrs767709505
23andMers767709505
23andMe allrs767709505
SNP Nexus

SNPshotrs767709505
SNPdbers767709505
MSV3drs767709505
GWAS Ctlgrs767709505
Max Magnitude0
ClinVar
Risk rs767709505(A;A)
Alt rs767709505(A;A)
Reference rs767709505(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89868914C>T
CLNSRC
CLNACC RCV000188664.2,