Have questions? Visit https://www.reddit.com/r/SNPedia

rs755544706

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755544706(A;A)
Make rs755544706(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318641
GenePOLG
is asnp
is mentioned by
dbSNPrs755544706
ebirs755544706
HLIrs755544706
Exacrs755544706
Varsomers755544706
Maprs755544706
PheGenIrs755544706
hapmaprs755544706
1000 genomesrs755544706
hgdprs755544706
ensemblrs755544706
gopubmedrs755544706
geneviewrs755544706
scholarrs755544706
googlers755544706
pharmgkbrs755544706
gwascentralrs755544706
openSNPrs755544706
23andMers755544706
23andMe allrs755544706
SNP Nexus

SNPshotrs755544706
SNPdbers755544706
MSV3drs755544706
GWAS Ctlgrs755544706
Max Magnitude0
ClinVar
Risk rs755544706(A;A)
Alt rs755544706(A;A)
Reference rs755544706(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861872G>A
CLNSRC
CLNACC RCV000188620.2,