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rs775168496

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775168496(A;A)
Make rs775168496(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89322800
GenePOLG
is asnp
is mentioned by
dbSNPrs775168496
ebirs775168496
HLIrs775168496
Exacrs775168496
Varsomers775168496
Maprs775168496
PheGenIrs775168496
hapmaprs775168496
1000 genomesrs775168496
hgdprs775168496
ensemblrs775168496
gopubmedrs775168496
geneviewrs775168496
scholarrs775168496
googlers775168496
pharmgkbrs775168496
gwascentralrs775168496
openSNPrs775168496
23andMers775168496
23andMe allrs775168496
SNP Nexus

SNPshotrs775168496
SNPdbers775168496
MSV3drs775168496
GWAS Ctlgrs775168496
Max Magnitude0
ClinVar
Risk rs775168496(A;A)
Alt rs775168496(A;A)
Reference rs775168496(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89866031G>A
CLNSRC
CLNACC RCV000188574.1,