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rs767339769

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767339769(C;T)
Make rs767339769(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320856
GenePOLG
is asnp
is mentioned by
dbSNPrs767339769
ebirs767339769
HLIrs767339769
Exacrs767339769
Varsomers767339769
Maprs767339769
PheGenIrs767339769
hapmaprs767339769
1000 genomesrs767339769
hgdprs767339769
ensemblrs767339769
gopubmedrs767339769
geneviewrs767339769
scholarrs767339769
googlers767339769
pharmgkbrs767339769
gwascentralrs767339769
openSNPrs767339769
23andMers767339769
23andMe allrs767339769
SNP Nexus

SNPshotrs767339769
SNPdbers767339769
MSV3drs767339769
GWAS Ctlgrs767339769
Max Magnitude0
ClinVar
Risk rs767339769(T;T)
Alt rs767339769(T;T)
Reference rs767339769(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89864087C>T
CLNSRC
CLNACC RCV000188592.1,