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rs202039305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202039305(A;A)
Make rs202039305(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position89333553
GenePOLG
is asnp
is mentioned by
dbSNPrs202039305
dbSNP (old)rs202039305
ClinGenrs202039305
ebirs202039305
HLIrs202039305
Exacrs202039305
Gnomadrs202039305
Varsomers202039305
LitVarrs202039305
Maprs202039305
PheGenIrs202039305
Biobankrs202039305
1000 genomesrs202039305
hgdprs202039305
ensemblrs202039305
gopubmedrs202039305
geneviewrs202039305
scholarrs202039305
googlers202039305
pharmgkbrs202039305
gwascentralrs202039305
openSNPrs202039305
23andMers202039305
23andMe allrs202039305
SNPshotrs202039305
SNPdbers202039305
MSV3drs202039305
GWAS Ctlgrs202039305
Max Magnitude0
ClinVar
Risk rs202039305(A;A)
Alt rs202039305(A;A)
Reference Rs202039305(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89876784G>A
CLNSRC
CLNACC RCV000296330.1,