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rs200309005

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200309005(C;T)
Make rs200309005(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320832
GenePOLG
is asnp
is mentioned by
dbSNPrs200309005
ebirs200309005
HLIrs200309005
Exacrs200309005
Varsomers200309005
Maprs200309005
PheGenIrs200309005
hapmaprs200309005
1000 genomesrs200309005
hgdprs200309005
ensemblrs200309005
gopubmedrs200309005
geneviewrs200309005
scholarrs200309005
googlers200309005
pharmgkbrs200309005
gwascentralrs200309005
openSNPrs200309005
23andMers200309005
23andMe allrs200309005
SNP Nexus

SNPshotrs200309005
SNPdbers200309005
MSV3drs200309005
GWAS Ctlgrs200309005
Max Magnitude0
ClinVar
Risk rs200309005(T;T)
Alt rs200309005(T;T)
Reference rs200309005(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89864063C>T
CLNSRC
CLNACC RCV000188594.2,