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rs796052892

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052892(A;A)
Make rs796052892(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89319356
GenePOLG
is asnp
is mentioned by
dbSNPrs796052892
ebirs796052892
HLIrs796052892
Exacrs796052892
Varsomers796052892
Maprs796052892
PheGenIrs796052892
hapmaprs796052892
1000 genomesrs796052892
hgdprs796052892
ensemblrs796052892
gopubmedrs796052892
geneviewrs796052892
scholarrs796052892
googlers796052892
pharmgkbrs796052892
gwascentralrs796052892
openSNPrs796052892
23andMers796052892
23andMe allrs796052892
SNP Nexus

SNPshotrs796052892
SNPdbers796052892
MSV3drs796052892
GWAS Ctlgrs796052892
Max Magnitude0
ClinVar
Risk rs796052892(A;A)
Alt rs796052892(A;A)
Reference rs796052892(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89862587G>T
CLNSRC
CLNACC RCV000188596.1,