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rs760431841

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs760431841(G;G)
Make rs760431841(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320944
GenePOLG
is asnp
is mentioned by
dbSNPrs760431841
ebirs760431841
HLIrs760431841
Exacrs760431841
Varsomers760431841
Maprs760431841
PheGenIrs760431841
hapmaprs760431841
1000 genomesrs760431841
hgdprs760431841
ensemblrs760431841
gopubmedrs760431841
geneviewrs760431841
scholarrs760431841
googlers760431841
pharmgkbrs760431841
gwascentralrs760431841
openSNPrs760431841
23andMers760431841
23andMe allrs760431841
SNP Nexus

SNPshotrs760431841
SNPdbers760431841
MSV3drs760431841
GWAS Ctlgrs760431841
Max Magnitude0
ClinVar
Risk rs760431841(G;G)
Alt rs760431841(G;G)
Reference rs760431841(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89864175T>A
CLNSRC
CLNACC RCV000188588.1,