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rs141367015

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141367015(C;G)
Make rs141367015(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89330081
GenePOLG
is asnp
is mentioned by
dbSNPrs141367015
ebirs141367015
HLIrs141367015
Exacrs141367015
Varsomers141367015
Maprs141367015
PheGenIrs141367015
hapmaprs141367015
1000 genomesrs141367015
hgdprs141367015
ensemblrs141367015
gopubmedrs141367015
geneviewrs141367015
scholarrs141367015
googlers141367015
pharmgkbrs141367015
gwascentralrs141367015
openSNPrs141367015
23andMers141367015
23andMe allrs141367015
SNP Nexus

SNPshotrs141367015
SNPdbers141367015
MSV3drs141367015
GWAS Ctlgrs141367015
Max Magnitude0
ClinVar
Risk rs141367015(G;G)
Alt rs141367015(G;G)
Reference rs141367015(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89873312C>G
CLNSRC
CLNACC RCV000188644.2,