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rs769410130

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769410130(A;A)
Make rs769410130(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89329051
GenePOLG
is asnp
is mentioned by
dbSNPrs769410130
ebirs769410130
HLIrs769410130
Exacrs769410130
Varsomers769410130
Maprs769410130
PheGenIrs769410130
hapmaprs769410130
1000 genomesrs769410130
hgdprs769410130
ensemblrs769410130
gopubmedrs769410130
geneviewrs769410130
scholarrs769410130
googlers769410130
pharmgkbrs769410130
gwascentralrs769410130
openSNPrs769410130
23andMers769410130
23andMe allrs769410130
SNP Nexus

SNPshotrs769410130
SNPdbers769410130
MSV3drs769410130
GWAS Ctlgrs769410130
Max Magnitude0
ClinVar
Risk rs769410130(A;A)
Alt rs769410130(A;A)
Reference rs769410130(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89872282G>C
CLNSRC
CLNACC RCV000188649.1,