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rs368435864

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368435864(C;T)
Make rs368435864(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318736
GenePOLG
is asnp
is mentioned by
dbSNPrs368435864
ebirs368435864
HLIrs368435864
Exacrs368435864
Varsomers368435864
Maprs368435864
PheGenIrs368435864
hapmaprs368435864
1000 genomesrs368435864
hgdprs368435864
ensemblrs368435864
gopubmedrs368435864
geneviewrs368435864
scholarrs368435864
googlers368435864
pharmgkbrs368435864
gwascentralrs368435864
openSNPrs368435864
23andMers368435864
23andMe allrs368435864
SNP Nexus

SNPshotrs368435864
SNPdbers368435864
MSV3drs368435864
GWAS Ctlgrs368435864
Max Magnitude0
ClinVar
Risk rs368435864(A,T;A,T)
Alt rs368435864(A,T;A,T)
Reference rs368435864(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861967C>A; NC_000015.9:g.89861967C>T
CLNSRC
CLNACC RCV000188616.2, RCV000188614.1,