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rs56047213

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56047213(C;T)
Make rs56047213(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89318617
GenePOLG
is asnp
is mentioned by
dbSNPrs56047213
ebirs56047213
HLIrs56047213
Exacrs56047213
Varsomers56047213
Maprs56047213
PheGenIrs56047213
hapmaprs56047213
1000 genomesrs56047213
hgdprs56047213
ensemblrs56047213
gopubmedrs56047213
geneviewrs56047213
scholarrs56047213
googlers56047213
pharmgkbrs56047213
gwascentralrs56047213
openSNPrs56047213
23andMers56047213
23andMe allrs56047213
SNP Nexus

SNPshotrs56047213
SNPdbers56047213
MSV3drs56047213
GWAS Ctlgrs56047213
Max Magnitude0
ClinVar
Risk rs56047213(T;T)
Alt rs56047213(T;T)
Reference rs56047213(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.89861848C>T
CLNSRC
CLNACC RCV000188615.2,