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rs753410045

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753410045(C;T)
Make rs753410045(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318710
GenePOLG
is asnp
is mentioned by
dbSNPrs753410045
ebirs753410045
HLIrs753410045
Exacrs753410045
Varsomers753410045
Maprs753410045
PheGenIrs753410045
hapmaprs753410045
1000 genomesrs753410045
hgdprs753410045
ensemblrs753410045
gopubmedrs753410045
geneviewrs753410045
scholarrs753410045
googlers753410045
pharmgkbrs753410045
gwascentralrs753410045
openSNPrs753410045
23andMers753410045
23andMe allrs753410045
SNP Nexus

SNPshotrs753410045
SNPdbers753410045
MSV3drs753410045
GWAS Ctlgrs753410045
Max Magnitude0
ClinVar
Risk rs753410045(T;T)
Alt rs753410045(T;T)
Reference rs753410045(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861941C>G
CLNSRC
CLNACC RCV000188617.1,