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rs113994093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994093(A;A)
Make rs113994093(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position89330241
GenePOLG
is asnp
is mentioned by
dbSNPrs113994093
ebirs113994093
HLIrs113994093
Exacrs113994093
Varsomers113994093
Maprs113994093
PheGenIrs113994093
hapmaprs113994093
1000 genomesrs113994093
hgdprs113994093
ensemblrs113994093
gopubmedrs113994093
geneviewrs113994093
scholarrs113994093
googlers113994093
pharmgkbrs113994093
gwascentralrs113994093
openSNPrs113994093
23andMers113994093
23andMe allrs113994093
SNP Nexus

SNPshotrs113994093
SNPdbers113994093
MSV3drs113994093
GWAS Ctlgrs113994093
Max Magnitude0
ClinVar
Risk rs113994093(A;A)
Alt rs113994093(A;A)
Reference rs113994093(G;G)
Significance Pathogenic
Disease Mitochondrial diseases
Variation info
Gene POLG
CLNDBN Mitochondrial diseases
Reversed 1
HGVS NC_000015.9:g.89873472C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020483.1,