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rs548076633

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs548076633(C;C)
Make rs548076633(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318553
GenePOLG
is asnp
is mentioned by
dbSNPrs548076633
ebirs548076633
HLIrs548076633
Exacrs548076633
Varsomers548076633
Maprs548076633
PheGenIrs548076633
hapmaprs548076633
1000 genomesrs548076633
hgdprs548076633
ensemblrs548076633
gopubmedrs548076633
geneviewrs548076633
scholarrs548076633
googlers548076633
pharmgkbrs548076633
gwascentralrs548076633
openSNPrs548076633
23andMers548076633
23andMe allrs548076633
SNP Nexus

SNPshotrs548076633
SNPdbers548076633
MSV3drs548076633
GWAS Ctlgrs548076633
Max Magnitude0
ClinVar
Risk rs548076633(C;C)
Alt rs548076633(C;C)
Reference rs548076633(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861784T>C
CLNSRC
CLNACC RCV000188622.1,