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rs1057517891

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517891(C;T)
Make rs1057517891(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position89333346
GenePOLG
is asnp
is mentioned by
dbSNPrs1057517891
dbSNP (old)rs1057517891
ClinGenrs1057517891
ebirs1057517891
HLIrs1057517891
Exacrs1057517891
Gnomadrs1057517891
Varsomers1057517891
Maprs1057517891
PheGenIrs1057517891
Biobankrs1057517891
1000 genomesrs1057517891
hgdprs1057517891
ensemblrs1057517891
gopubmedrs1057517891
geneviewrs1057517891
scholarrs1057517891
googlers1057517891
pharmgkbrs1057517891
gwascentralrs1057517891
openSNPrs1057517891
23andMers1057517891
23andMe allrs1057517891
SNPshotrs1057517891
SNPdbers1057517891
MSV3drs1057517891
GWAS Ctlgrs1057517891
Max Magnitude0
ClinVar
Risk rs1057517891(T;T)
Alt rs1057517891(T;T)
Reference Rs1057517891(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89876577G>A
CLNSRC
CLNACC RCV000414240.1,