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

rs368587966

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs368587966(C;C)
Make rs368587966(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89321223
GenePOLG
is asnp
is mentioned by
dbSNPrs368587966
ebirs368587966
HLIrs368587966
Exacrs368587966
Varsomers368587966
Maprs368587966
PheGenIrs368587966
hapmaprs368587966
1000 genomesrs368587966
hgdprs368587966
ensemblrs368587966
gopubmedrs368587966
geneviewrs368587966
scholarrs368587966
googlers368587966
pharmgkbrs368587966
gwascentralrs368587966
openSNPrs368587966
23andMers368587966
23andMe allrs368587966
SNP Nexus

SNPshotrs368587966
SNPdbers368587966
MSV3drs368587966
GWAS Ctlgrs368587966
Max Magnitude0
ClinVar
Risk rs368587966(C;C)
Alt rs368587966(C;C)
Reference rs368587966(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89864454T>C
CLNSRC
CLNACC RCV000188586.1,