Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052889

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052889(A;A)
Make rs796052889(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position89321773
GenePOLG
is asnp
is mentioned by
dbSNPrs796052889
ebirs796052889
HLIrs796052889
Exacrs796052889
Varsomers796052889
Maprs796052889
PheGenIrs796052889
hapmaprs796052889
1000 genomesrs796052889
hgdprs796052889
ensemblrs796052889
gopubmedrs796052889
geneviewrs796052889
scholarrs796052889
googlers796052889
pharmgkbrs796052889
gwascentralrs796052889
openSNPrs796052889
23andMers796052889
23andMe allrs796052889
SNP Nexus

SNPshotrs796052889
SNPdbers796052889
MSV3drs796052889
GWAS Ctlgrs796052889
Max Magnitude0
ClinVar
Risk rs796052889(A;A)
Alt rs796052889(A;A)
Reference rs796052889(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene POLG
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.89865004G>T
CLNSRC
CLNACC RCV000188584.1,