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rs796052899

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052899(C;T)
Make rs796052899(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89333327
GeneLOC105370962, POLG
is asnp
is mentioned by
dbSNPrs796052899
ebirs796052899
HLIrs796052899
Exacrs796052899
Varsomers796052899
Maprs796052899
PheGenIrs796052899
hapmaprs796052899
1000 genomesrs796052899
hgdprs796052899
ensemblrs796052899
gopubmedrs796052899
geneviewrs796052899
scholarrs796052899
googlers796052899
pharmgkbrs796052899
gwascentralrs796052899
openSNPrs796052899
23andMers796052899
23andMe allrs796052899
SNP Nexus

SNPshotrs796052899
SNPdbers796052899
MSV3drs796052899
GWAS Ctlgrs796052899
Max Magnitude0
ClinVar
Risk rs796052899(T;T)
Alt rs796052899(T;T)
Reference rs796052899(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89876558G>A
CLNSRC
CLNACC RCV000188634.1,