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rs764036283

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs764036283(A;G)
Make rs764036283(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318676
GenePOLG
is asnp
is mentioned by
dbSNPrs764036283
ebirs764036283
HLIrs764036283
Exacrs764036283
Varsomers764036283
Maprs764036283
PheGenIrs764036283
hapmaprs764036283
1000 genomesrs764036283
hgdprs764036283
ensemblrs764036283
gopubmedrs764036283
geneviewrs764036283
scholarrs764036283
googlers764036283
pharmgkbrs764036283
gwascentralrs764036283
openSNPrs764036283
23andMers764036283
23andMe allrs764036283
SNP Nexus

SNPshotrs764036283
SNPdbers764036283
MSV3drs764036283
GWAS Ctlgrs764036283
Max Magnitude0
ClinVar
Risk rs764036283(G;G)
Alt rs764036283(G;G)
Reference rs764036283(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861907A>G
CLNSRC
CLNACC RCV000188619.2,