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rs769637557

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs769637557(G;G)
Make rs769637557(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89327004
GeneMIR6766, POLG
is asnp
is mentioned by
dbSNPrs769637557
ebirs769637557
HLIrs769637557
Exacrs769637557
Varsomers769637557
Maprs769637557
PheGenIrs769637557
hapmaprs769637557
1000 genomesrs769637557
hgdprs769637557
ensemblrs769637557
gopubmedrs769637557
geneviewrs769637557
scholarrs769637557
googlers769637557
pharmgkbrs769637557
gwascentralrs769637557
openSNPrs769637557
23andMers769637557
23andMe allrs769637557
SNP Nexus

SNPshotrs769637557
SNPdbers769637557
MSV3drs769637557
GWAS Ctlgrs769637557
Max Magnitude0
ClinVar
Risk rs769637557(G;G)
Alt rs769637557(G;G)
Reference rs769637557(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MIR6766 POLG
CLNDBN not specified
Reversed 0
HGVS NC_000015.9:g.89870235T>G
CLNSRC
CLNACC RCV000188661.2,