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rs367610201

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs367610201(A;G)
Make rs367610201(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89325591
GenePOLG
is asnp
is mentioned by
dbSNPrs367610201
ebirs367610201
HLIrs367610201
Exacrs367610201
Varsomers367610201
Maprs367610201
PheGenIrs367610201
hapmaprs367610201
1000 genomesrs367610201
hgdprs367610201
ensemblrs367610201
gopubmedrs367610201
geneviewrs367610201
scholarrs367610201
googlers367610201
pharmgkbrs367610201
gwascentralrs367610201
openSNPrs367610201
23andMers367610201
23andMe allrs367610201
SNP Nexus

SNPshotrs367610201
SNPdbers367610201
MSV3drs367610201
GWAS Ctlgrs367610201
Max Magnitude0
ClinVar
Risk rs367610201(G;G)
Alt rs367610201(G;G)
Reference rs367610201(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89868822A>G
CLNSRC
CLNACC RCV000188667.1,