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rs1057517803

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517803(C;T)
Make rs1057517803(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position89330113
GenePOLG
is asnp
is mentioned by
dbSNPrs1057517803
dbSNP (old)rs1057517803
ClinGenrs1057517803
ebirs1057517803
HLIrs1057517803
Exacrs1057517803
Gnomadrs1057517803
Varsomers1057517803
Maprs1057517803
PheGenIrs1057517803
Biobankrs1057517803
1000 genomesrs1057517803
hgdprs1057517803
ensemblrs1057517803
gopubmedrs1057517803
geneviewrs1057517803
scholarrs1057517803
googlers1057517803
pharmgkbrs1057517803
gwascentralrs1057517803
openSNPrs1057517803
23andMers1057517803
23andMe allrs1057517803
SNPshotrs1057517803
SNPdbers1057517803
MSV3drs1057517803
GWAS Ctlgrs1057517803
Max Magnitude0
ClinVar
Risk rs1057517803(T;T)
Alt rs1057517803(T;T)
Reference Rs1057517803(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89873344G>A
CLNSRC
CLNACC RCV000414708.1,