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rs762972003

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762972003(A;A)
Make rs762972003(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89320833
GenePOLG
is asnp
is mentioned by
dbSNPrs762972003
ebirs762972003
HLIrs762972003
Exacrs762972003
Varsomers762972003
Maprs762972003
PheGenIrs762972003
hapmaprs762972003
1000 genomesrs762972003
hgdprs762972003
ensemblrs762972003
gopubmedrs762972003
geneviewrs762972003
scholarrs762972003
googlers762972003
pharmgkbrs762972003
gwascentralrs762972003
openSNPrs762972003
23andMers762972003
23andMe allrs762972003
SNP Nexus

SNPshotrs762972003
SNPdbers762972003
MSV3drs762972003
GWAS Ctlgrs762972003
Max Magnitude0
ClinVar
Risk rs762972003(A,T;A,T)
Alt rs762972003(A,T;A,T)
Reference rs762972003(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene POLG
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.89864064G>A
CLNSRC
CLNACC RCV000188593.2,