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rs201732356

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201732356(A;A)
Make rs201732356(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318737
GenePOLG
is asnp
is mentioned by
dbSNPrs201732356
ebirs201732356
HLIrs201732356
Exacrs201732356
Varsomers201732356
Maprs201732356
PheGenIrs201732356
hapmaprs201732356
1000 genomesrs201732356
hgdprs201732356
ensemblrs201732356
gopubmedrs201732356
geneviewrs201732356
scholarrs201732356
googlers201732356
pharmgkbrs201732356
gwascentralrs201732356
openSNPrs201732356
23andMers201732356
23andMe allrs201732356
SNP Nexus

SNPshotrs201732356
SNPdbers201732356
MSV3drs201732356
GWAS Ctlgrs201732356
Max Magnitude0
ClinVar
Risk rs201732356(A,C;A,C)
Alt rs201732356(A,C;A,C)
Reference rs201732356(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861968G>A; NC_000015.9:g.89861968G>C
CLNSRC
CLNACC RCV000188613.1, RCV000188612.1,